Non-Invasive Vagus Nerve Stimulator For Migraine Headache

FDA classification

FDA Class 2 ·Non-Invasive Vagus Nerve Stimulator For Migraine Headache

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM

MODIFIED C-DAK

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

C-DAK 3500

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

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

AccuPoint Electrode

FDA 510(k)

FDA Class 2 ·Neurology

Synvitro Hyadase

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

CERAMAX

FDA 510(k)

FDA Class 2 ·Dental

C-DAK ARTIFICIAL KIDNEY

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

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/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/L INTERBODY FUSION SYSTEM

C-DAK 2100 ARTIFICIAL KIDNEY

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

BAK-ON SP PORCELAIN ALLOY

FDA 510(k)

FDA Class 2 ·Dental

KIDNEY, ARTIFICIAL, C-DAK 2.0

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

ARTIFICIAL KIDNEY, C-DAK 0.6D

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology