510(k) K020761 ยท HRX Arthroscope
POWER TEK II
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Apr 3, 2002 |
| Received | Mar 7, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020761
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.