510(k) K962215 ยท HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER
| Applicant | U.S. Medical Products, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Aug 15, 1996 |
| Received | Jun 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962215
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.