510(k) K062310 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
REFLEX HYBRID ACP SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 18, 2006 |
| Received | Aug 8, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062310
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 12, 2010 | Stryker Spine Stryker Reflex Hybrid Screw Extractor;
Not Sterile: Manufactured by: Stryker Spine SAS,
Cestas, France; Distributed in the USA by: Stryker Spine, 2 Pearl Court, Allendale, NJ.
The threaded tip of the Terminated |
KWQ | None listed |
| Apr 12, 2010 | Stryker Spine Stryker Reflex Hybrid Screw Extractor Inner Shaft;
Not Sterile;
Manufactured by: Stryker Spine SAS, Cestas, France;
Distributed in the US by: Stryker Spine, 2 Pearl Court, Allendale, NJ.
The threaded Terminated |
KWQ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.