ZIMMER BONE CEMENT CENTRIFUGATION SYS— 510(k) K843219
Substantially EquivalentZimmer, Inc.
FDA 510(k) clearance K843219 for ZIMMER BONE CEMENT CENTRIFUGATION SYS, Substantially Equivalent on 1984-11-29. Applicant: Zimmer, Inc.. Device class: 1.
Clearance details
- Applicant
- Zimmer, Inc.
- Product code
- Code JDZ
- Device class
- Class 1
- Regulation
- 21 CFR 888.4210
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Recent devices under product code JDZ
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- K251840 — Zimmer® Persona® Personalized Knee System
- K260182 — Avenir® Müller Stem; Avenir Complete Hip System
- K253592 — Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
Adverse events under product code JDZ
product code JDZ- Malfunction
- 461
- Total
- 461
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.