510(k) K052123 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNTHES PANGEA SYSTEM
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Sep 23, 2005 |
| Received | Aug 5, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052123
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.