SEARCH RESULTS FOR: Origin(20 results)

Company Name

• SpineArt SA (9)
• CURITEVA, INC. (5)
• Cutting Edge Spine, LLC (1)
• Innovasis, Inc. (1)
• MET 1 TECHNOLOGIES, LLC (1)
• NVISION BIOMEDICAL TECHNOLOGIES, INC. (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)
• EARP Interbody System (1)
• ENDOSKELETON® TCS (1)
• EVOL®ha-C Cervical Interbody System (1)
• JULIET ® Ti LL Instrumentation (1)
• KODIAK PL TL GRAFT BLOCK (1)
• TRYPTIK CC INSTRUMENTATION (1)
• icotec Lumbar Cage, Implant Holder for Tamping (1)

GMDN Term Name

• Bone graft packing block (19)
• Polymeric spinal interbody fusion cage (1)

GMDN Term Status

• Active (20)

FDA Product Code Name

• Intervertebral Fusion Device With Bone Graft, Lumbar (12)
• Intervertebral Fusion Device With Bone Graft, Cervical (7)
• Intervertebral fusion device with bone graft, cervical (2)
• Intervertebral Fusion Device With Integrated Fixation, Lumbar (1)
• Intervertebral fusion device with integrated fixation, cervical (1)

FDA Product Code

• ODP (9)
• MAX (12)
• OVD (1)
• OVE (1)

Device Packaged As Sterile

• No (20)

Sterilization Prior To Use

• Yes (20)

Issuing Agency

• GS1 (14)
• HIBCC (6)

Device Size

• Depth: 14 Millimeter (1)
• Height: 1 Inch (1)
• Height: 8 Millimeter (1)
• Length: 1.5 Inch (1)
• Length: 50 Millimeter (1)
• Width: 2 Inch (1)
• Width: 25 Millimeter (1)

Device Class

• Class II (20)

Implantable

• No (19)
• Yes (1)