510(k) K925995 ยท HRX Arthroscope
ARTHREX INSTRUMENTS (KNEE, GP 3)
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 4, 1993 |
| Received | Nov 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925995
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.