510(k) K971289 ยท KWP Appliance, Fixation, Spinal Interlaminal
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
| Applicant | Osteotech, Inc., Eatontown NJ, US |
| Decision | Substantially Equivalent, Jun 18, 1997 |
| Received | Apr 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971289
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.