510(k) K082504 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
APOLLO ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Apollo Spine, Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Jan 27, 2009 |
| Received | Aug 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082504
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.