510(k) K061002 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MAXIMA ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | U&I Corp., Uijungbu, Gyeonggi-Do, KR |
| Decision | Substantially Equivalent, Nov 15, 2006 |
| Received | Apr 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061002
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.