BEUDAMED
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    SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APR-T REVISION STEM LT 11MM

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWY·November 4, 1997

    POR STM TIB B/P LT SZ1 NK II

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code HSH·May 3, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·June 4, 2002

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·March 20, 2001

    NATURAL KNEE

    FDA Adverse Event
    SULZER ORTHOPEDICS, INC.·Product code JWH·October 21, 2000

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·May 3, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·April 18, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·April 20, 2001

    SULZER ORTHOPEDICS, INC

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·August 30, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS, INC.·Product code KWB·February 26, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·October 5, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·April 20, 2001

    HEMI POR SHL W/SEALED SCWHLS SZ55MM I-O

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·April 20, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·May 21, 2001

    FEMORAL STEM, SIZE 3

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC·Product code KWY·August 20, 2003

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS INC.·Product code KWB·February 26, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS, INC.·Product code KWB·January 3, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·June 18, 2001

    HEMI POR SHL W/SEALED SCWHLS SZ51MM I-O

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·April 20, 2001