FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)

K Number: K253592 · Decision Apr 13, 2026
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
36
Applicant Total
376
Review Days
147

Basic Information

Device Name
Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
K Number
K253592
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3670
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer, Inc.
Date Received
November 17, 2025
Decision Date
April 13, 2026
Product Code
MBF
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

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