Traditional bunion

correction surgery

Put bunions in their place.

Once and for all.

Bunions are a pain — literally. But one simple procedure could change it all. Welcome to Lapifuse, a type of bunion surgical correction that is designed to reduce pain and increase mobility.1,2 With Lapifuse, patients are less likely to experience bunion recurrence.1

Improved appearance

Bunion correction treatment that removes the bunion and preserves the length of the toe to protect the natural appearance of the foot

Pain reduction

The LapiFuse procedure is designed to reduce pain and the likelihood of future procedures1,2 by eliminating the bunion and maintaining the alignment achieved during the procedure.

Improved mobility

Specifically designed to improve mobility by addressing the issue in the midfoot, which preserves the joint movement of the big toe, allowing you to get back to your active lifestyle.

How does it work?

The time required for the LapiFuse procedure is unique to each patient and surgeon. Generally, the LapiFuse procedure will take 45-60 minutes. During the procedure, your surgeon will make a few small incisions to expose the affected joint. After preparing the joint, they will then rotate the joint to return it to its proper alignment, restoring the foot to its natural appearance. To secure the correction, your surgeon will apply anatomically correct titanium plates, to the joint.

Recovery instructions may vary by surgeon, and results are specific to individual patients. Your surgeon may recommend that you keep your foot elevated to heal for the first week post-procedure; then after 10 days, your surgeon may place a bunion dressing and short walker boot. After 6 weeks, your doctor may decide if it is appropriate to remove the boot and you may be able to wear normal footwear. Please consult your doctor on recovery instructions to ensure optimal healing.

Find a surgeon in your region to help you find the right solution for you.

FAQs

Some bunion correction procedures require shortening of the toe and large incisions that can affect how the foot looks, while potentially creating new pain and leading to additional surgical procedures.
The LapiFuse Bunion Procedure is designed to preserve toe length, reduce pain and restore the natural appearance of the foot.2

The time required for the LapiFuse procedure is unique to each patient and surgeon. Generally, the LapiFuse procedure will take 45-60 minutes.

Recovery timelines vary depending on the procedure and your surgeon's protocol.3 In the early post-operative period, a patient may be advised to keep the foot elevated to reduce swelling4 and may be instructed to limit weight bearing or walk on the heel while healing progresses.5 Transition back to regular footwear may occur over several weeks, as directed by a surgeon.3

Because the LapiFuse procedure preserves the joint movement of the big toe, it is specially designed to improve mobility, letting you get back to your active lifestyle. At the direction of their surgeon, some patients may be able to return to regular physical activity 6-7 weeks after their procedure. However, please consult your doctor on recovery instructions to ensure optimal healing. Recovery instructions may vary by surgeon. Results are specific to individual patients.

A doctor may allow a patient to resume full-weight bearing in loose fitting closed-toed shows at 6-7 weeks. Your doctor will provide you with recovery instructions to ensure optimal healing. Recovery instructions may vary by surgeon. Results are specific to individual patients.

Surgical correction of bunions seeks to address the underlying structural causes of bunions and the LapiFuse procedure is specially designed with compression technology to reduce the likelihood that bunions will return.1 However, there is a possibility that the bunions may return and, to reduce that risk, be sure to comply fully with your doctor’s recovery instructions.

Is LapiFuse right for me?

Use the discussion guide below when speaking with your doctor to determine if surgery is the right next step.

  • How long have you had bunions?

  • What non-surgical or at-home treatments have you use for temporary relief?

  • Does your bunion pain ever make it difficult to walk or stand for long periods of time?

  • Does your bunion pain ever prevent you from daily activities or exercise?

References:
  1. Galli MM, Protzman NM, Brigido SA. J Foot Ankle Surg. 2015;54(3):437-440. Accessed May 13, 2026.
  2. Walker JL, Harris EJ. Foot Ankle Clin. 2019;24(4):641-648. Accessed May 13, 2026.
  3. American Orthopaedic Foot & Ankle Society. Bunion surgery (hallux valgus) patient guide. FootCareMD. FootCareMD. Accessed May 13, 2026.
  4. Nix S, Smith M, Vicenzino B. Prevalence of hallux valgus and clinical considerations: a systematic review. J Foot Ankle Res. 2010;3:21. doi:10.1186/1757-1146-3-21
  5. University of Colorado School of Medicine. Post-operative bunionectomy protocol. University of Colorado Anschutz Medical Campus. Accessed May 13, 2026.
Important information

Bunion surgery is intended for individuals with deformities of the first metatarsophalangeal joint (the joint at the base of the big toe). Based on a determination jointly made by a patient and a healthcare professional in consideration of a patient’s unique clinical factors, bunion surgery may be appropriate for certain individuals, and certain products, like those discussed below, may be used for treatment.

The PROstep MICA Screw System is intended to be used for fixation of bone fractures (e.g., repair of broken bones) or bone reconstruction (e.g. restoring shape, alignment or structure of a damaged, deformed or surgically altered bone).

The Ortholoc 2 Lapidus with Rotation System is intended to be used for the stabilization and fixation of fresh fractures, revision procedures, joint fusion (joining together), and reconstruction of bones of the feet and toes. Specific examples include: Arthrodesis (surgical fusion) of the first metatarsal cuneiform joint (base joint of the big toe).

The ProStep MICA Screw System and the Ortholoc 2 Lapidus with Rotation System are intended for patients in generally good health. The area treated should have good blood flow and normal nerve function. The skin must be healthy enough to fully cover the implant. The muscles and tendons should be strong enough to support normal movement. The bone also needs to be strong enough to hold the implant securely.

The Ortholoc 2 Lapidus with Rotation System and the PROstep MICA Screw System are not appropriate for patients who have certain types of infections, physiologically or psychologically inadequate patients (patients who have certain mental health conditions or physical conditions that may make them inappropriate candidates for surgery), patients with irreparable tendon system (tendons are so damaged they cannot be repaired), growing patients with open epiphyses (patients who’s bones are still growing), patients with high levels of activity, or patients that may benefit from more conservative treatment (such as footwear modification or physical therapy).

Any surgery has serious risks. The risks associated with the aforementioned product systems and/or procedures include but are not limited to infection, pain, swelling, and inflammation around the implant. Certain implant-related risks which may lead to revision of the implant or additional surgeries include implant fracture (breakage), loosening, dislocation (moving out of place). Additional risks include bone resorption (bone loss) or bone over-production (extra bone growth), allergic reaction to the implant materials, untoward histological responses possibly involving macrophages and/or fibroblasts (the body, including the body’s cells and tissues, may react abnormally to the implant over time), migration of particle wear debris possibly resulting in a bodily response (small pieces of the implant may wear off and migrate through the body resulting in a reaction), and embolism (blocked blood vessel). Additionally, delayed union (bone is taking longer than expected to heal), non-union (failure of bone to heal) or failure of the implant could occur.

The information presented is for educational purposes only. Stryker is not dispensing medical advice. Please speak to your doctor to decide if bunion surgery is appropriate for you. Only your doctor can make the medical decision about which products and treatments are right for your own individual condition. As with any surgery, bunion surgery carries certain risks. Your surgeon will explain all the possible complications of the surgery, as well as side effects. Additionally, the lifetime of an implant is not infinite and varies with each individual. Also, each patient will experience a different post-operative activity level, depending on their own individual clinical factors. Your doctor will help counsel you about how to best maintain your activities to potentially prolong the lifetime of the device. It is important to closely follow your doctor's instructions regarding post-surgery activity, treatment and follow-up care.   

Stryker Corporation or its other divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: Mica, Ortholoc, PROstep, Stryker. All other trademarks are trademarks of their respective owners or holders. 

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