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

FDA 510(k) K251620 · Zimmer Biomet

Substantially Equivalent

510(k) numberK251620

Submission

Device name
A.L.P.S. Proximal Humerus Plating System
Applicant
Zimmer Biomet
Warsaw, IN, US
Received
May 27, 2025
Decision date
July 25, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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K261511Xpert AnkleHRS · Traditional Newclip Technics07/28/2026SE
K261406Versalock Proximal Tibial Plating SystemHRS · Traditional GM Dos Reis Industria e Comercio Ltda.07/21/2026SE
K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion…HRS · Special TriMed, Inc.07/16/2026SE
K261191Alians Elbow SHRS · Traditional Newclip Technics07/08/2026SE
K261054RibPlate SystemHRS · Traditional Stryker Leibinger GmbH & Co KG07/01/2026SE
K261351SALGINA 2.5mm Distal Radius SystemHRS · Traditional Bonebridge AG06/26/2026SE

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Questions and answers

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

A.L.P.S. Proximal Humerus Plating System (K251620) received a 510(k) decision of Substantially Equivalent on July 25, 2025, 59 days after the submission was received.

What is the product code of K251620?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.