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Dynesys Dynamic Stabilization System

Highridge Medical, LLC · Model 07.01299.001 · UDI-DI 03662663109871

NQP
10
510(k) clearances
848
Adverse events
50
Recalls
44
Facilities

Description

Guide, Set Screw

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, Switzerland, after receiv
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, Switzerland, after receiv
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, Switzerland, after receiv
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, Switzerland, after receiv
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, Switzerland, after receiv
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, Switzerland, after receiv
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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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.