Intervertebral fusion device with bone graft, lumbar

FDA registration

Acero Precision·1 product·🇺🇸 United States

Tibow

FDA registration

LIFE SPINE·1 product·🇺🇸 United States

TiBow

FDA registration

GIZMO PRECISION MEDICAL LLC·1 product·🇺🇸 United States

The TiBow Expandable Spacer System

FDA 510(k)

FDA Class 2 ·Orthopedic

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072016850·ARTHROGRAM PACK - 170919

Vue PACS

FDA registration

Philips India Limited - Radiology Informatics, Clinical Informatics, Patient Care Informatics Business Units·1 product·🇮🇳 India

Vue PACS

FDA registration

Philips Medical Systems Technologies Ltd.·1 product·🇮🇱 Israel

RespiConnect Adapter

FDA registration

TRUDELL MEDICAL INTERNATIONAL·1 product·🇨🇦 Canada

PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202

FDA 510(k)

FDA Class 2 ·Radiology

CARESTREAM PACS

FDA 510(k)

FDA Class 2 ·Radiology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

System, Imaging, Pulsed Doppler, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Doppler, Ultrasonic

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological