510(k) K022344 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Centerpulse Spine-Tech, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 24, 2002 |
| Received | Jul 19, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022344
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 24, 2005 | Zimmer Spine, Inc. Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spine Trinica Anterior Cervical Plating Instrument sets (catalog numbers 07.00215.001 and 07.00546.001). Terminated |
HWX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.