510(k) K050813 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ABC 2 SCREW
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, May 4, 2005 |
| Received | Mar 31, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050813
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.