510(k) K043181 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
| Applicant | Vertebron, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Dec 17, 2004 |
| Received | Nov 17, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K043181
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.