Interventional Cardiovascular Implant Simulation Software Device

FDA classification

FDA Class 2 ·Interventional Cardiovascular Implant Simulation Software Device

Implanted Tibial Electrical Urinary Continence Device

FDA classification

FDA Class 2 ·Implanted Tibial Electrical Urinary Continence Device

Catheter, Flow Directed

FDA Pre-Market Approval

FDA Class 2 ·VOYAGER OTW CORONARY DILATION CATHETER

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·VOYAGER RX CORONARY DILATATION CATHETER

Analyzer, Medical Image

FDA Pre-Market Approval

FDA Class 2 ·ICAD SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

Implantable Post-Surgical Kinematic Measurement Knee Device

FDA classification

FDA Class 2 ·Implantable Post-Surgical Kinematic Measurement Knee Device

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE

Active Implantable Bone Conduction Hearing System

FDA classification

FDA Class 2 ·Active Implantable Bone Conduction Hearing System

Sub-Scalp Implanted Electroencephalogram System For Remote Patient Monitoring

FDA classification

FDA Class 2 ·Sub-Scalp Implanted Electroencephalogram System For Remote Patient Monitoring

Defect Measurement Tool

FDA classification

FDA Class 2 ·Defect Measurement Tool

Instruments Designed For Press-Fit Osteochondral Implants

FDA classification

FDA Class 2 ·Instruments Designed For Press-Fit Osteochondral Implants

Shoulder Arthroplasty Implantation System

FDA classification

FDA Class 2 ·Shoulder Arthroplasty Implantation System

Knee Arthroplasty Implantation System

FDA classification

FDA Class 2 ·Knee Arthroplasty Implantation System

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·POWERSAIL(TM)/HIGHSAIL(TM) CORONARY DILATATION CATHETER

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·ACS RX SOLARIS CORONARY DILATATION CATHETER

Non-Coring (Huber) Needle

FDA classification

FDA Class 2 ·Non-Coring (Huber) Needle

Medial Knee Implanted Shock Absorber

FDA classification

FDA Class 2 ·Medial Knee Implanted Shock Absorber

Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation

FDA classification

FDA Class 2 ·Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation