P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT— 510(k) K924340
Substantially EquivalentJohnson & Johnson Orthopaedics, Inc.
FDA 510(k) clearance K924340 for P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT, Substantially Equivalent on 1994-01-25. Applicant: Johnson & Johnson Orthopaedics, Inc..
Clearance details
- Applicant
- Johnson & Johnson Orthopaedics, Inc.
- Product code
- Code JWH
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raynham, MA, US
Adverse events under product code JWH
product code JWH- Death
- 26
- Injury
- 51,564
- Malfunction
- 9,725
- Other
- 9
- Total
- 61,324
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.