510(k) K050804 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO: SPECTRUMTM CERVICAL SPINAL SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 11, 2005 |
| Received | Mar 30, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050804
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.