PRELUDE PF

FDA UDI

Biomet Sports Medicine, LLC·00880304676824·

KneeTec PFJ

FDA UDI

CORIN LTD·05056139210235·KneeTec PFJ Femoral implant Right Size 4

PRELUDE PF

FDA UDI

Biomet Orthopedics, LLC·00880304564329·

KineMatch® PFR System

FDA UDI

Kinamed, Inc.·00818720010847·PFR Left

NA

FDA UDI

Smith & Nephew, Inc.·03596010061225·TYPE II FEMORAL PATELLAR COMPONENT ...

JOURNEY

FDA UDI

Smith & Nephew, Inc.·03596010573315·JOURNEY PATELLOFEMORAL IMPLANT ...

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

WORKSTATION PLUS W/LOCAL AREA NETWORK(LAN) OPTION

FDA 510(k)

FDA Class 2 ·Cardiovascular

COMPACT MONITOR SMK 210,211,230,231,240

FDA 510(k)

FDA Class 2 ·Cardiovascular

SMU 611 VERS. 2.0 INCLUDING PRESSNI,DILU,SAT-MOD.

FDA 510(k)

FDA Class 2 ·Cardiovascular

CARDIAC THERAPHY SYSTEM SCP 900

FDA 510(k)

FDA Class 2 ·Cardiovascular

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512

FDA 510(k)

FDA Class 2 ·Cardiovascular

STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512

FDA 510(k)

FDA Class 2 ·Cardiovascular

ECG/RESPIRATION/ARRHYTHMIA MODULE FOR RM-301

FDA 510(k)

FDA Class 2 ·Cardiovascular

MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS.

FDA 510(k)

FDA Class 2 ·Cardiovascular