510(k) K121801 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
QUINTEX CERVICAL PLATING SYSTEM
| Applicant | Aesculap Implant Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Sep 11, 2012 |
| Received | Jun 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121801
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.