SEARCH RESULTS FOR: seaspine(35 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (35)

Brand Name

• SeaSpine Spacer System - Pacifica (7)
• Disc Prep (6)
• PLIF Allograft (4)
• SeaSpine Spacer System - Hollywood™ (4)
• Tether (4)
• Posterior Disc Prep (2)
• Steerable IBD (2)
• Zuma (2)
• Cambria (1)
• SeaSpine Spacer System - Ventura™ (1)
• Sierra™ (1)
• Vu ePOD™ (1)

GMDN Term Name

• Orthopaedic surgical distractor, internal (11)
• Bone file (10)
• Spinal implant trial (6)
• Orthopaedic implant driver (3)
• Bone curette, reusable (1)
• Bone tap, reusable (1)
• Cannulated surgical drill bit, single-use (1)
• Instrument tray, reusable (1)
• Orthopaedic implant inserter/extractor, reusable (1)

GMDN Term Status

• Active (25)
• Obsolete (10)

FDA Product Code Name

• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (12)
• RASP (8)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (6)
• BIT, DRILL (3)
• Intervertebral fusion device with bone graft, lumbar (3)
• CUTTER, SURGICAL (2)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• CURETTE (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)
• Orthopedic tray (1)
• TAP, BONE (1)

FDA Product Code

• LXH (12)
• HTR (8)
• MQP (6)
• HTW (3)
• MAX (3)
• FZT (2)
• HTF (1)
• HWX (1)
• KWP (1)
• MNI (1)
• OJH (1)

Device Packaged As Sterile

• No (35)

Sterilization Prior To Use

• Yes (35)

Issuing Agency

• GS1 (35)

Device Size Type

• 13mm (35)

Device Class

• Class I (28)
• Class II (7)

Implantable

• No (35)