Identity Shoulder System— 510(k) K250848
Substantially EquivalentZimmer, Inc.
FDA 510(k) clearance K250848 for Identity Shoulder System, Substantially Equivalent on 2025-07-02. Applicant: Zimmer, Inc.. Device class: 2.
Clearance details
- Applicant
- Zimmer, Inc.
- Product code
- Code MBF
- Device class
- Class 2
- Regulation
- 21 CFR 888.3670
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Recent devices under product code MBF
view all- K253592 — Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
- K251098 — Identity Revision Humeral Stems
- K240876 — Identity Shoulder System
- K233712 — PRIMA Humeral System; PRIMA TT Glenoid
- K231099 — SMR Hybrid Glenoid System
More clearances from Zimmer, Inc.
view allAdverse events under product code MBF
product code MBF- Injury
- 597
- Total
- 597
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.