BEUDAMED
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    VITOSS BONE GRAFT SUBSTITUTE

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code MQV·May 18, 2012

    IMBIBE BONE MARROW ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code KNW·May 18, 2012

    CELLPAKER COLLECTION DEVICE

    FDA Adverse Event
    Malfunction ·ORTHOVITA, INC.·Product code LMF·May 18, 2012

    VITAGEL SURGICAL HEMOSTAT

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LMF·May 18, 2012

    VITAGEL SURGICAL HEMOSTAT

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LMF·May 18, 2012

    VITOSS FOAM PACK

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LYC·April 17, 2007

    VITOSS FOAM PACK

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LYC·April 17, 2007

    VITOSS FOAM PACK

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LYC·April 17, 2007

    VITOSS FOAM PACK

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LYC·April 17, 2007

    VITAGEL SURGICAL HEMOSTAT

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code LMF·August 29, 2011

    ALIQUOT SYRINGE DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code KIH·August 29, 2011

    ALIQUOT SYRINGE DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code NDN·August 3, 2011

    FILLER, BONE VOID, CALCIUM COMPOUND

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code MQV·September 14, 2011

    CORTOSS BONE AUGMENTATION MATERIAL

    FDA Adverse Event
    Malfunction ·ORTHOVITA, INC.·Product code NDN·September 28, 2011

    CORTOSS BONE AUGMENTATION MATERIAL

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code NDN·November 1, 2010

    CORTOSS BONE AUGMENTATION MATERIAL

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code NDN·November 1, 2010

    FILLER, BONE VOID, CALCIUM COMPOUND

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code MQV·September 14, 2011

    ALIQUOT SYRINGE DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code OAR·August 3, 2011

    ALIQUOT SYRINGE DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code OAR·August 3, 2011

    VITOSS

    FDA Adverse Event
    Injury ·ORTHOVITA, INC.·Product code MQV·August 12, 2023