ZIMMER BONE CEMENT CENTRIFUGATION SYS— 510(k) K843219

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K843219 for ZIMMER BONE CEMENT CENTRIFUGATION SYS, Substantially Equivalent on 1984-11-29. Applicant: Zimmer, Inc..

Clearance details

Applicant
Zimmer, Inc.
Product code
Code JDZ
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Warsaw, IN, US
Download summary PDFView on FDA.gov ↗

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.