510(k) K950501 ยท HRX Arthroscope
DANEK RIGID ARTHROSCOPE
| Applicant | Sofamor Danek USA,Inc., Memphis TN, US |
| Decision | Substantially Equivalent, May 12, 1995 |
| Received | Feb 6, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950501
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.