510(k) K033844 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SYNTHES ANTERIOR CERVICAL COMPRESSION SYSTEM
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Feb 5, 2004 |
| Received | Dec 11, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033844
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.