BEUDAMED
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    NEXGEN LEGACY LPS ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·April 21, 2011

    CLOSURE TOP

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code KWP·July 20, 2015

    TRINICA SCREW SELF-DRILLING VARIABLE 4.2X14

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code KWQ·January 26, 2012

    FLEXPOSURE

    FDA Adverse Event
    Other ·ZIMMER SPINE, INC.·Product code LXH·January 9, 2009

    DYNESYS TOP LOADING

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code LXH·February 6, 2009

    CANNULATED POLYAXIAL SCREW 6.5MM X 35MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code NKB·April 7, 2014

    SEQUOIA AND PATHFINDER NXT CLOSURE TOP

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code NKB·June 5, 2014

    *

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC·Product code MAX·May 1, 2014

    ARDIS PEEK IMPLANT 08X09X22

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·June 20, 2014

    3.5MM X 24MM PRIMARY OPEN POLY SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code NKB·April 11, 2014

    TRINICA SCREW SELF-DRILLING VARIABLE 4.2X14

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWQ·May 14, 2014

    SPECIALTY HEX DRIVER, RING RETAINER

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·March 3, 2010

    SILHOUETTE PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code NKB·June 25, 2010

    TITLE2

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·April 23, 2010

    SEQUOIA SCREWDRIVER, MODULAR

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·May 27, 2010

    VIRAGE,POLYAXIAL SCREW 5.0X30MM

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code KWP·July 20, 2015

    ARDIS INSERTER - 9MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·June 17, 2014

    CLOSURE TOP

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code KWP·October 24, 2014

    SEQUOIA AND PATHFINDER NXT CLOSURE TOP

    FDA Adverse Event
    Injury ·ZIMMER SPINE, INC.·Product code NKB·December 18, 2014

    ARDIS PEEK IMPLANT 12X09X26

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·December 18, 2014