510(k) K130912 ยท HRX Arthroscope
OMNICUT RESECTION BLADE
| Applicant | Depuy Mitek, A Johnson & Johnson Company, Raynham MA, US |
| Decision | Substantially Equivalent, Jun 14, 2013 |
| Received | Apr 2, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130912
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.