510(k) K941691 ยท HRX Arthroscope
REVO ROTATOR CUFF REPAIR SYSTEM
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Sep 6, 1994 |
| Received | Apr 6, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941691
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.