510(k) K991662 ยท KWP Appliance, Fixation, Spinal Interlaminal
TITANIUM HARTSHILL SYSTEM
| Applicant | Surgicraft , Ltd., Redditch, Worcs., GB |
| Decision | Substantially Equivalent, Nov 8, 1999 |
| Received | May 14, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991662
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.