SEARCH RESULTS FOR: seaspine(26 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (26)

Brand Name

• Lateral Retractor (7)
• Daytona (6)
• NewPort (5)
• NewPort™ (3)
• BodyForm™ Thoraco-Lumbar (1)
• Cabo (1)
• Newport (1)
• Sonoma™ (1)
• Tether™ (1)

GMDN Term Name

• Bone-screw internal spinal fixation system, non-sterile (10)
• Orthopaedic retractor (9)
• Spinal fixation plate, non-bioabsorbable (4)
• Orthopaedic bone pin, non-bioabsorbable (2)
• Orthopaedic implant inserter/extractor, reusable (1)

GMDN Term Status

• Active (17)
• Obsolete (9)

FDA Product Code Name

• RETRACTOR (9)
• Thoracolumbosacral pedicle screw system (6)
• ORTHOSIS, SPINAL PEDICLE FIXATION (4)
• Orthosis, spinal pedicle fixation, for degenerative disc disease (4)
• Orthosis, spondylolisthesis spinal fixation (4)
• APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY (3)
• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (3)
• Appliance, fixation, spinal intervertebral body (1)

FDA Product Code

• NKB (10)
• GAD (9)
• KWQ (4)
• MNH (4)
• MNI (4)
• LXH (3)

Device Packaged As Sterile

• No (26)

Sterilization Prior To Use

• Yes (26)

Issuing Agency

• GS1 (26)

Device Size Type

• 80mm (26)

Device Class

• Class II (14)
• Class I (12)

Implantable

• Yes (16)
• No (10)