510(k) K132324 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SKYLINE ANTERIOR CERVICAL PLATE SYSTEM, UNIPLATE ANTERIOR CERVICAL PLATE SYSTEM, UNIPLATE 2 ANTERIOR CERVICAL PLATE SYST
| Applicant | Medos International SARL, Raynham MA, US |
| Decision | Substantially Equivalent, Sep 6, 2013 |
| Received | Jul 26, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132324
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.