510(k) K955927 ยท KWP Appliance, Fixation, Spinal Interlaminal
BRYAN POSTERIOR SPINAL FIXATOR (MODIFICATION)
| Applicant | Arcan Orthopaedic Corp., Ogden UT, US |
| Decision | Substantially Equivalent for Some Indications, Mar 13, 1996 |
| Received | Dec 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955927
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.