SEARCH RESULTS FOR: seaspine(23 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (23)

Brand Name

• Cabo (7)
• SeaSpine Spacer System - Hollywood™ (4)
• Zuma™ (3)
• Spinous Process System (2)
• Coral (1)
• SeaSpine Spacer System - Ventura™ (1)
• Sierra™ (1)
• Sonoma™ (1)
• Tether™ (1)
• Vu ePOD™ (1)
• Zuma-L™ (1)

GMDN Term Name

• Spinal fixation plate, non-bioabsorbable (11)
• Spinal implant trial (7)
• Bone-screw internal spinal fixation system, non-sterile (1)
• Cannulated surgical drill bit, single-use (1)
• Interspinous spinal fixation implant (1)
• Orthopaedic implant inserter/extractor, reusable (1)
• Vertebral body prosthesis, non-sterile (1)

GMDN Term Status

• Active (22)
• Obsolete (1)

FDA Product Code Name

• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (10)
• Appliance, fixation, spinal intervertebral body (7)
• APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY (3)
• Intervertebral fusion device with bone graft, lumbar (3)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (2)
• Intervertebral fusion device with integrated fixation, lumbar (2)
• ORTHOSIS, SPINAL PEDICLE FIXATION (2)
• Spinous process plate (2)
• Orthosis, spinal pedicle fixation, for degenerative disc disease (1)
• Orthosis, spondylolisthesis spinal fixation (1)

FDA Product Code

• KWQ (10)
• MQP (10)
• MAX (3)
• KWP (2)
• MNI (2)
• OVD (2)
• PEK (2)
• MNH (1)
• NKB (1)

Device Packaged As Sterile

• No (23)

Sterilization Prior To Use

• Yes (23)

Issuing Agency

• GS1 (23)

Device Size Type

• 16mm (23)

Device Class

• Class II (23)

Implantable

• Yes (13)
• No (10)