510(k) K953387 ยท HRX Arthroscope
ECTRA LIGAMENT RELEASE SYSTEM
| Applicant | Smith & Nephew Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Aug 9, 1995 |
| Received | Jul 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953387
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.