K240876
- 510(k) number
- K240876
- Device name
- Identity Shoulder System
- Applicant
- Zimmer, Inc. IN · US
- Product code
- MBF — Prosthesis, Shoulder, Semi-Constrained, Metal/Polyme
- Decision date
- 2024-06-12
- Date received
- 2024-03-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K240876.pdf
Official FDA record: K240876
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.