SEARCH RESULTS FOR: Origin(23 results)

Company Name

• SpineArt SA (10)
• CURITEVA, INC. (5)
• Altus Spine, LLC (1)
• Choice Spine, LP (1)
• Cutting Edge Spine, LLC (1)
• Innovasis, Inc. (1)
• Life Spine, Inc. (1)
• MET 1 TECHNOLOGIES, LLC (1)
• TITAN SPINE, LLC (1)
• icotec AG (1)

Brand Name

• JULIET INSTRUMENTATION (5)
• Savant Lumbar Interbody Fusion System (3)
• Sage Cervical Interbody Fusion System (2)
• TRYPTIK ® TI (2)
• CxHA™ (1)
• ENDOSKELETON® TCS (1)
• EVOL®ha-C Cervical Interbody System (1)
• HARRIER-SA Lumbar Interbody System (1)
• Imola-Silverstone (1)
• JULIET ® Ti LL Instrumentation (1)
• KODIAK PL TL GRAFT BLOCK (1)
• Plateau-C Ti (1)
• SCARLET® AC-Ti (1)
• TRYPTIK CC INSTRUMENTATION (1)
• icotec Lumbar Cage, Implant Holder for Tamping (1)

GMDN Term Name

• Bone graft packing block (23)

GMDN Term Status

• Active (23)

FDA Product Code Name

• Intervertebral Fusion Device With Bone Graft, Lumbar (11)
• Intervertebral Fusion Device With Bone Graft, Cervical (8)
• Intervertebral fusion device with bone graft, cervical (3)
• Intervertebral fusion device with bone graft, lumbar (2)
• Intervertebral Fusion Device With Integrated Fixation, Cervical (1)
• Intervertebral Fusion Device With Integrated Fixation, Lumbar (1)
• Intervertebral fusion device with integrated fixation, cervical (1)
• Intervertebral fusion device with integrated fixation, lumbar (1)

FDA Product Code

• MAX (13)
• ODP (11)
• OVD (2)
• OVE (2)

Device Packaged As Sterile

• No (23)

Sterilization Prior To Use

• Yes (23)

Issuing Agency

• GS1 (17)
• HIBCC (6)

Device Size

• Height: 1 Inch (1)
• Length: 1.5 Inch (1)
• Length: 50 Millimeter (1)
• Width: 2 Inch (1)

Device Class

• Class II (23)

Implantable

• No (23)