510(k) K913561 ยท KWP Appliance, Fixation, Spinal Interlaminal
LUQUE SEGMENTAL SPINAL INSTRUMENTATION
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 16, 1992 |
| Received | Aug 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913561
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.