FDA Device Intelligence
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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

Recent recalls

DateFirmReason
2012-09-04Zimmer, 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
2012-09-04Zimmer, 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
2012-09-04Zimmer, 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
2012-09-04Zimmer, 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
2012-09-04Zimmer, 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
2012-09-04Zimmer, 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
2009-05-28Zimmer Inc.The spacer cutter may jam during surgery, preventing use of the instrument and causing surgical delay.
2009-02-09Synthes USA (HQ), Inc.package integrity compromised
2009-02-09Synthes USA (HQ), Inc.package integrity compromised
2009-02-09Synthes USA (HQ), Inc.package integrity compromised

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.