510(k) K901765 ยท HRX Arthroscope
POSTEROMEDIAL GUIDE
| Applicant | Smith & Nephew Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jun 25, 1990 |
| Received | Apr 18, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901765
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.