510(k) K954014 ยท HRX Arthroscope
PERCUTANEOUS DISCECTOMY CANNULA SYSTEM
| Applicant | T. Korossurgical Instruments Corp., Moorepark CA, US |
| Decision | Substantially Equivalent for Some Indications, Nov 6, 1995 |
| Received | Aug 25, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954014
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.