SEARCH RESULTS FOR: seaspine(26 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (26)

Brand Name

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

GMDN Term Name

• Orthopaedic surgical distractor, internal (9)
• Bone file (8)
• Spinal implant trial (5)
• Bone curette, reusable (1)
• Cannulated surgical drill bit, single-use (1)
• Instrument tray, reusable (1)
• Orthopaedic implant inserter/extractor, reusable (1)

GMDN Term Status

• Active (18)
• Obsolete (8)

FDA Product Code Name

• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (10)
• RASP (7)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (6)
• Intervertebral fusion device with bone graft, lumbar (3)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• CURETTE (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)
• Orthopedic tray (1)

FDA Product Code

• LXH (10)
• HTR (7)
• MQP (6)
• MAX (3)
• HTF (1)
• KWP (1)
• MNI (1)
• OJH (1)

Device Packaged As Sterile

• No (26)

Sterilization Prior To Use

• Yes (26)

Issuing Agency

• GS1 (26)

Device Size Type

• 15mm (26)

Device Class

• Class I (19)
• Class II (7)

Implantable

• No (26)