K253592

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

510(k) number
K253592
Device name
Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
Applicant
Zimmer, Inc. IN · US
Product code
MBF — Prosthesis, Shoulder, Semi-Constrained, Metal/Polyme
Decision date
2026-04-13
Date received
2025-11-17
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain

Also available from FDA: K253592.pdf

Official FDA record: K253592
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.