SEARCH RESULTS FOR: Origin(21 results)

Company Name

• SpineArt SA (21)

Brand Name

• JULIET INSTRUMENTATION (7)
• JULIET ® INSTRUMENTATION (3)
• ROMEO 2 PAD INSTRUMENTATION (2)
• SCARLET AL-T INSTRUMENTATION (2)
• TRYPTIK ® TI (2)
• JULIET ® Ti LL Instrumentation (1)
• PERLA TL (1)
• PERLA ® TL MIS (1)
• SCARLET AC-T INSTRUMENTATION (1)
• TRYPTIK CC INSTRUMENTATION (1)

GMDN Term Name

• Bone graft packing block (21)

GMDN Term Status

• Active (21)

FDA Product Code Name

• Intervertebral Fusion Device With Bone Graft, Lumbar (6)
• Orthopedic Manual Surgical Instrument (4)
• Instrument, Compression (3)
• Intervertebral Fusion Device With Bone Graft, Cervical (3)
• Spinous Process Plate (2)
• Appliance, Fixation, Spinal Interlaminal (1)
• Impactor (1)
• Intervertebral Fusion Device With Integrated Fixation, Cervical (1)
• Intervertebral Fusion Device With Integrated Fixation, Lumbar (1)
• Thoracolumbosacral Pedicle Screw System (1)

FDA Product Code

• MAX (6)
• LXH (4)
• HWN (3)
• ODP (3)
• PEK (2)
• HWA (1)
• KWP (1)
• NKB (1)
• OVD (1)
• OVE (1)

Device Packaged As Sterile

• No (21)

Sterilization Prior To Use

• Yes (21)

Issuing Agency

• GS1 (21)

Device Class

• Class II (13)
• Class I (8)

Implantable

• No (21)