Home › Device types › NQP
Posterior Metal/Polymer Spinal System, Fusion
FDA product code NQP · Class 2 · Orthopedic
2,484
Registered devices
848
Adverse events
50
Recalls
22
510(k) clearances
Devices with this code
TRANSITION — GLOBUS MEDICAL, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.TRANSITION — GLOBUS MEDICAL, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.TRANSITION — GLOBUS MEDICAL, INC.TRANSITION — GLOBUS MEDICAL, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.Dynesys® — Zimmer GmbHDynesys® — Zimmer GmbHDSS HP Polyaxial pedicle screw set, Ø7 x 30mm — Paradigm Spine GmbHCD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.Dynesys® Top-Loading System — Zimmer GmbHDynesys® — Zimmer GmbHCD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switz |
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switz |
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switz |
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switz |
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switz |
| 2012-09-04 | Zimmer, Inc. | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthru, Switz |
| 2009-05-28 | Zimmer Inc. | The spacer cutter may jam during surgery, preventing use of the instrument and causing surgical delay. |
| 2009-02-09 | Synthes USA (HQ), Inc. | package integrity compromised |
| 2009-02-09 | Synthes USA (HQ), Inc. | package integrity compromised |
| 2009-02-09 | Synthes USA (HQ), Inc. | package integrity compromised |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
