510(k) K091689 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNAPSE SYSTEM 4.0MM, OC FUSION SYSTEM 4.0MM
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Jul 10, 2009 |
| Received | Jun 10, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091689
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.