Precice™ Max System and Precice™ Ankle Salvage System
K-Number: K261651 · 2026-06-18
Device Summary
Frequently Asked Questions
What is the Precice™ Max System and Precice™ Ankle Salvage System?
Precice™ Max System and Precice™ Ankle Salvage System is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is NuVasive Specialized Orthopedics. The 510(k) number is K261651.
When did Precice™ Max System and Precice™ Ankle Salvage System receive FDA 510(k) clearance?
Precice™ Max System and Precice™ Ankle Salvage System received FDA 510(k) clearance on 2026-06-18, under 510(k) number K261651.
Who is the listed applicant for Precice™ Max System and Precice™ Ankle Salvage System?
The FDA 510(k) record lists NuVasive Specialized Orthopedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Precice™ Max System and Precice™ Ankle Salvage System?
The FDA product code for Precice™ Max System and Precice™ Ankle Salvage System is HSB.
Other records listing NuVasive Specialized Orthopedics as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HSB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.