510(k) K051815 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
| Applicant | Vertebron, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Oct 17, 2005 |
| Received | Jul 5, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051815
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.