SEARCH RESULTS FOR: Origin(14 results)

Company Name

• SpineArt SA (14)

Brand Name

• JULIET INSTRUMENTATION (5)
• ROMEO 2 PAD INSTRUMENTATION (2)
• TRYPTIK ® TI (2)
• JULIET ® Ti LL Instrumentation (1)
• PERLA ® TL MIS (1)
• SCARLET AC-T INSTRUMENTATION (1)
• SCARLET® AC-Ti (1)
• TRYPTIK CC INSTRUMENTATION (1)

GMDN Term Name

• Bone graft packing block (14)

GMDN Term Status

• Active (14)

FDA Product Code Name

• Intervertebral Fusion Device With Bone Graft, Lumbar (6)
• Intervertebral Fusion Device With Bone Graft, Cervical (4)
• Intervertebral Fusion Device With Integrated Fixation, Cervical (2)
• Spinous Process Plate (2)
• Appliance, Fixation, Spinal Interlaminal (1)
• Intervertebral Fusion Device With Integrated Fixation, Lumbar (1)
• Thoracolumbosacral Pedicle Screw System (1)

FDA Product Code

• MAX (6)
• ODP (4)
• OVE (2)
• PEK (2)
• KWP (1)
• NKB (1)
• OVD (1)

Device Packaged As Sterile

• No (14)

Sterilization Prior To Use

• Yes (14)

Issuing Agency

• GS1 (14)

Device Class

• Class II (14)

Implantable

• No (14)