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FDA 510(k)

A.L.P.S. Proximal Humerus Plating System

K-Number: K251620 · 2025-07-25

ApplicantZimmer Biomet
Decision Date2025-07-25
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A.L.P.S. Proximal Humerus Plating System is a medical device manufactured by Zimmer Biomet. It received FDA 510(k) clearance on 2025-07-25 under approval number K251620. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.L.P.S. Proximal Humerus Plating System?

A.L.P.S. Proximal Humerus Plating System is a medical device that received FDA 510(k) clearance on 2025-07-25. It is manufactured by Zimmer Biomet. The 510(k) number is K251620.

When was A.L.P.S. Proximal Humerus Plating System approved by the FDA?

A.L.P.S. Proximal Humerus Plating System received FDA 510(k) clearance on 2025-07-25, under approval number K251620.

What company makes A.L.P.S. Proximal Humerus Plating System?

A.L.P.S. Proximal Humerus Plating System is manufactured by Zimmer Biomet.

What is the FDA product code for A.L.P.S. Proximal Humerus Plating System?

The FDA product code for A.L.P.S. Proximal Humerus Plating System is HRS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.