SEARCH RESULTS FOR: seaspine(42 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (42)

Brand Name

• Disc Prep (7)
• Laminoplasty (6)
• Shoreline ASC (6)
• Steerable IBD (4)
• Sierra (3)
• Cambria (2)
• Posterior Disc Prep (2)
• Spinous Process System (2)
• Zuma-C™ (2)
• Integra Expandable Interbody (1)
• NewPort (1)
• Regatta Lateral System (1)
• SeaSpine Expandable Interbody (1)
• Sierra™ (1)
• Skipjack (1)
• Vu cPOD (1)
• Zuma-C (1)

GMDN Term Name

• Vertebral body prosthesis, non-sterile (7)
• Orthopaedic surgical distractor, internal (6)
• Bone file/rasp, manual, reusable (5)
• Bone file (4)
• Instrument tray, reusable (3)
• Spinal fixation plate, non-bioabsorbable (3)
• Spinal implant trial (3)
• Orthopaedic implant inserter/extractor, reusable (2)
• Surgical screwdriver, reusable (2)
• Bone tap, reusable (1)
• Cannulated surgical drill bit, single-use (1)
• Interspinous spinal fixation implant (1)
• Ophthalmic knife, reusable (1)
• Orthopaedic implantation sleeve, reusable (1)
• Orthopaedic joint/limb rongeur (1)
• Surgical drill guide, reusable (1)

GMDN Term Status

• Active (31)
• Obsolete (11)

FDA Product Code Name

• RASP (9)
• Intervertebral fusion device with integrated fixation, cervical (8)
• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (8)
• Intervertebral fusion device with bone graft, lumbar (3)
• ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL (3)
• Orthopedic tray (3)
• BIT, DRILL (2)
• Spinous process plate (2)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• Guide, surgical, instrument (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)
• RONGEUR (1)
• TAP, BONE (1)

FDA Product Code

• HTR (9)
• LXH (8)
• OVE (8)
• MAX (3)
• NQW (3)
• OJH (3)
• HTW (2)
• PEK (2)
• FZX (1)
• HTX (1)
• HWX (1)
• KWP (1)
• MNI (1)

Device Packaged As Sterile

• No (42)

Sterilization Prior To Use

• Yes (42)

Issuing Agency

• GS1 (42)

Device Size Type

• 6mm (42)

Device Class

• Class I (25)
• Class II (17)

Implantable

• No (38)
• Yes (4)