510(k) K965221 ยท KWP Appliance, Fixation, Spinal Interlaminal
RANSFORD CERVICAL FIXATION SYSTEM
| Applicant | Surgicraft , Ltd., Redditch, Worcestershire, GB |
| Decision | Substantially Equivalent, Aug 7, 1997 |
| Received | Dec 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965221
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.