510(k) K073120 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
ACCIN PATELLOFEMORAL SYSTEM
| Applicant | Accelerated Innovation, LLC, Clifton NJ, US |
| Decision | Substantially Equivalent, Feb 29, 2008 |
| Received | Nov 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073120
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.