29 results · 22ms · Sources: EU EUDAMED, US FDA

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ACCUSYTE 3D Fiducial Marker

FDA 510(k)
FDA Class 2 ·Radiology

X-CORE

FDA UDI
Nuvasive, Inc.·00887517426505·X-CORE 2 Ti Core, Ø18x21-27mm

FINN KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304005402·

Fixation Screw

FDA UDI
I.T.S. GmbH·09120047297117·Fixation Screw, Proximal Lateral Tibia Plate

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009375·PedFuse, Adjustable Cross Connector, Angled, 55mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009344·PedFuse, Adjustable Cross Connector, Angled, 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009351·PedFuse, Adjustable Cross Connector, Angled, 35mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009368·PedFuse, Adjustable Cross Connector, Angled, 45mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009382·PedFuse, Adjustable Cross Connector, Angled, 75mm

SURGICAL FACE MASK; SURGICAL FACE MASK

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

PILAIRO NASAL PILLOWS MASK

FDA 510(k)
FDA Class 2 ·Anesthesiology

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) X System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·FRED X System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·FRED

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) and FRED X System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System, FREDX System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED) and FRED X System

Intracranial Aneurysm Flow Diverter

FDA Pre-Market Approval
FDA Class 3 ·Flow Re-Direction Endoluminal Device (FRED®) System