INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA registration

ZAVATION·1 product·🇺🇸 United States

Bradshaw Medical Inc.

FDA registration

Bradshaw Medical Inc.·1 product·🇺🇸 United States

FLXFIT INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

Oticon

FDA UDI

Oticon A/S·05707131264657·RIA PRO, KIT 312 WL DIR 85 R V BE

SOPRO 281 LED LIGHT SOURCE

FDA registration

SOPRO·2 products·🇫🇷 France

MICRUS MODIFIED MICROCOIL SYSTEM, "CERECYTE"

FDA registration

MEDOS INTERNATIONAL SARL·1 product·🇨🇭 Switzerland

VC150

FDA registration

INNOKAS MEDICAL OY·1 product·🇫🇮 Finland

Stryker Mako

FDA registration

Phillips Precision Inc·2 products·🇺🇸 United States

MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE

FDA 510(k)

FDA Class 2 ·Neurology

SOPRO 281

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Led Light Source

FDA classification

FDA Class 2 ·Led Light Source

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Device, Neurovascular Embolization

FDA classification

FDA Class 2 ·Device, Neurovascular Embolization