SEARCH RESULTS FOR: seaspine(32 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (32)

Brand Name

• Daytona (14)
• Newport (4)
• Coral (3)
• BodyForm™ (1)
• BodyForm™ Thoraco-Lumbar (1)
• Cabo (1)
• Hollywood™ (1)
• Integra Expandable Interbody (1)
• NewPort (1)
• SeaSpine Expandable Interbody (1)
• SeaSpine Spacer System - Hollywood (1)
• SeaSpine Spacer System - Hollywood NanoMetalene (1)
• SeaSpine® Spacer System - Redondo (1)
• Zuma-L (1)

GMDN Term Name

• Bone-screw internal spinal fixation system, non-sterile (21)
• Instrument tray, reusable (5)
• Spinal fixation plate, non-bioabsorbable (3)
• Bone file (1)
• Orthopaedic implant inserter/extractor, reusable (1)
• Vertebral body prosthesis, non-sterile (1)

GMDN Term Status

• Active (30)
• Obsolete (2)

FDA Product Code Name

• Thoracolumbosacral pedicle screw system (14)
• ORTHOSIS, SPINAL PEDICLE FIXATION (7)
• Orthosis, spinal pedicle fixation, for degenerative disc disease (7)
• Orthosis, spondylolisthesis spinal fixation (7)
• APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY (5)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (3)
• Intervertebral fusion device with bone graft, lumbar (3)
• Orthopedic tray (3)
• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (2)
• Appliance, fixation, spinal intervertebral body (1)
• Intervertebral fusion device with bone graft, cervical (1)

FDA Product Code

• NKB (21)
• MNH (7)
• MNI (7)
• KWQ (6)
• KWP (3)
• MAX (3)
• OJH (3)
• LXH (2)
• ODP (1)

Device Packaged As Sterile

• No (32)

Sterilization Prior To Use

• Yes (32)

Issuing Agency

• GS1 (32)

Device Size Type

• 30mm (32)

Device Class

• Class II (27)
• Class I (5)

Implantable

• Yes (24)
• No (8)