SEARCH RESULTS FOR: seaspine(23 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (21)
• Seaspine, Inc. (2)

Brand Name

• Shoreline ASC (6)
• SeaSpine Spacer System - Hollywood™ (4)
• Laminoplasty (3)
• Spinous Process System (2)
• UCR (2)
• Zuma-C™ (2)
• SeaSpine Spacer System - Ventura™ (1)
• Sierra™ (1)
• Vu ePOD™ (1)
• Zuma-L™ (1)

GMDN Term Name

• Spinal implant trial (7)
• Vertebral body prosthesis, non-sterile (7)
• Spinal fixation plate, non-bioabsorbable (4)
• Bone-screw internal spinal fixation system, non-sterile (2)
• Cannulated surgical drill bit, single-use (1)
• Interspinous spinal fixation implant (1)
• Orthopaedic implant inserter/extractor, reusable (1)

GMDN Term Status

• Active (16)
• Obsolete (7)

FDA Product Code Name

• Intervertebral fusion device with integrated fixation, cervical (8)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (7)
• Intervertebral fusion device with bone graft, lumbar (3)
• ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL (3)
• Appliance, Fixation, Spinal Interlaminal (2)
• Orthosis, Spinal Pedicle Fixation (2)
• Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease (2)
• Orthosis, Spondylolisthesis Spinal Fixation (2)
• Spinous process plate (2)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• Intervertebral fusion device with integrated fixation, lumbar (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)

FDA Product Code

• OVE (8)
• MQP (7)
• KWP (3)
• MAX (3)
• MNI (3)
• NQW (3)
• MNH (2)
• NKB (2)
• PEK (2)
• OVD (1)

Device Packaged As Sterile

• No (23)

Sterilization Prior To Use

• Yes (23)

Issuing Agency

• GS1 (23)
• HIBCC (2)

Device Size Type

• 8mm (23)

Device Class

• Class II (23)

Implantable

• No (16)
• Yes (7)