510(k) K014090 ยท KWP Appliance, Fixation, Spinal Interlaminal
ENDIUS SPINAL FIXATION SYSTEM
| Applicant | Endius, Inc., Plainville MA, US |
| Decision | Substantially Equivalent, Mar 11, 2002 |
| Received | Dec 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014090
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.