510(k) K072672 ยท NKB Thoracolumbosacral Pedicle Screw System
SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
| Applicant | Abbott Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Nov 28, 2007 |
| Received | Sep 21, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072672
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 29, 2011 | Zimmer Inc. Sequoia final driver closure top retention, non-sterile, REF 3384-2, Zimmer Spine, Austin, Texas, The device is used to apply final torque to closure tops of the implant.
The Sequoia Final Driver is Terminated |
HAO | None listed |
| Jul 23, 2008 | Abbott Spine Sequoia Spinal System Surgical Kits; Pedicle screw spinal system; Non-sterile (kits intended to be sterilized prior to use); Rx Only;
The Sequoia Spinal System is designed to aid in the surgical cor Terminated |
NKB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.