COONRAD III TOTAL ELBOW— 510(k) K883665
Substantially Equivalent for Some IndicationsZimmer, Inc.
FDA 510(k) clearance K883665 for COONRAD III TOTAL ELBOW, Substantially Equivalent for Some Indications on 1989-02-03. Applicant: Zimmer, Inc..
Clearance details
- Applicant
- Zimmer, Inc.
- Product code
- Code JDC
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Adverse events under product code JDC
product code JDC- Injury
- 1,050
- Total
- 1,050
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.