510(k) K972233 ยท HWC Screw, Fixation, Bone
STRYKER WEDGE INTERFERENCE SCREW SYSTEM
| Applicant | Stryker Endoscopy, Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 5, 1997 |
| Received | Jun 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972233
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 17, 2017 | Stryker Corporation STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled sterile. Terminated |
HWC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.