SPINAL ELEMENTS, INC.

FDA registration

SPINAL ELEMENTS, INC.·1 product·🇺🇸 United States

Lucent Intervertebral Body Fusion Device

FDA 510(k)

FDA Class 2 ·Orthopedic

Anterolateral Tibiaplate

FDA registration

I.T.S. GMBH·1 product·🇦🇹 Austria

Smith & Nephew, Inc.

FDA registration

ARVATO Netherlands B.V.·1 product·🇳🇱 Netherlands

Smith and Nephew

FDA registration

ARVATO USA LLC·1 product·🇺🇸 United States

OsteoMed

FDA UDI

OSTEOMED LLC·00842528128930·2.0mm x 11mm Cannulated Headless Screw

LACTOSORB* 2.0MM SYSTEM

FDA UDI

BIOMET MICROFIXATION, INC·00841036053949·

LEONE SPA

FDA UDI

LEONE SPA·08033707013914·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 11

ECLIPSE TREATMENT PLANNING SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

PILONPLATE WITH ANGULAR STABILITY

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

System, Planning, Radiation Therapy Treatment

FDA classification

FDA Class 2 ·System, Planning, Radiation Therapy Treatment

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone