510(k) K080790 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO THEKEN ATOLL CERVICO-THORACIC SYSTEM
| Applicant | Theken Spine, LLC, Akron OH, US |
| Decision | Substantially Equivalent, Apr 29, 2008 |
| Received | Mar 20, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080790
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.