K250848
- 510(k) number
- K250848
- Device name
- Identity Shoulder System
- Applicant
- Zimmer, Inc. IN · US
- Product code
- MBF — Prosthesis, Shoulder, Semi-Constrained, Metal/Polyme
- Decision date
- 2025-07-02
- Date received
- 2025-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K250848.pdf
Official FDA record: K250848
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.