510(k) K103819 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PSL ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Precision Surgery , Ltd., Chesterland OH, US |
| Decision | Substantially Equivalent, Feb 15, 2011 |
| Received | Dec 30, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103819
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.