510(k) K100265 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
DIAMOND ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Amendia, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, May 13, 2010 |
| Received | Jan 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100265
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.