BEUDAMED
    29 results · 39ms · Sources: EU EUDAMED, US FDA

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    INTERMEDICS ORTHOPEDICS REAMERS

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    INTERMEDICS ORTHOPEDICS DRILL BITS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    INTERMEDICS ORTHOPEDICS SAW BLADE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    INTERMEDICS ORTHOPEDICS-SULZER

    FDA Adverse Event
    Malfunction ·INTERMEDICS ORTHOPEDICS-SULZER·Product code JWH·January 24, 2002

    APR SCREWS, APR HIP SYSTEM

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code LZO·March 27, 1996

    INTERMEDICS

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS·Product code HSH·May 14, 1997

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    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS·Product code KWB·May 9, 1998

    NATURAL KNEE II TIBIAL INSERT IMPACTOR HEAD

    FDA Adverse Event
    Other ·INTERMEDICS ORTHOPEDICS, INC.·Product code HSH·August 27, 1996

    HIP PROSTHESIS

    FDA Adverse Event
    Malfunction ·INTERMEDICS ORTHOPEDICS, INC.·Product code KWY·June 11, 1996

    TOTAL KNEE REPLACEMENT

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code HRY·May 13, 1992

    NATURAL KNEE II NON-POROUS STEMMED TIBIA BASEPLATE

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code HSH·October 10, 1996

    NATURAL KNEE IDE PATELLA SZI

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code HTG·November 12, 1996

    APR HOODED PROTRUSION ENHANCED INSERT 28MM/57MM

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code KWB·November 20, 1996

    UNI-KNEE TIBIA INSERT 9MM SIZE 3.4

    FDA Adverse Event
    Other ·INTERMEDICS ORTHOPEDICS, INC.·Product code HRY·December 18, 1996

    NATURAL KNEE II NON-POROUS FEMORAL RT S25

    FDA Adverse Event
    Other ·INTERMEDICS ORTHOPEDICS, INC.·Product code HSA·November 7, 1996

    APR HOODED PROTRUSIO ENHANCED INSERT 26MM/47MM

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code KWB·November 20, 1996

    SELECT SHOULDER COCR HUMERAL HEAD

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code HSD·November 6, 1996

    UNI-KNEE TIBIAL INSERT 13 MM SIZE 3/4

    FDA Adverse Event
    Injury ·INTERMEDIC ORTHOPEDICS, INC.·Product code HSH·November 20, 1996

    NK IDE PATELLA

    FDA Adverse Event
    Injury ·INTERMEDICS ORTHOPEDICS, INC.·Product code HTG·October 10, 1996

    NATURAL KNEE TIBIA INSERT LEFT SIZE A/7MM

    FDA Adverse Event
    Other ·INTERMEDICS ORTHOPEDICS, INC.·Product code HSH·January 28, 1997