K253592
- 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.