SEARCH RESULTS FOR: seaspine(41 results)

Company Name

• Seaspine Orthopedics Corporation (41)

Brand Name

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

GMDN Term Name

• Bone file (10)
• Orthopaedic surgical distractor, internal (9)
• Spinal implant trial (7)
• Metal-polymer composite spinal interbody fusion cage (5)
• Bone file/rasp, manual, reusable (3)
• Vertebral body prosthesis, non-sterile (2)
• Bone curette, reusable (1)
• Cannulated surgical drill bit, single-use (1)
• Orthopaedic implant driver (1)
• Orthopaedic inorganic implant inserter/extractor, reusable (1)
• Surgical drill guide, reusable (1)

GMDN Term Status

• Active (29)
• Obsolete (12)

FDA Product Code Name

• RASP (11)
• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (10)
• Intervertebral fusion device with integrated fixation, cervical (8)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (6)
• Intervertebral fusion device with bone graft, lumbar (3)
• CUTTER, SURGICAL (2)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• CURETTE (1)
• Guide, surgical, instrument (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)
• SCREWDRIVER (1)

FDA Product Code

• HTR (11)
• LXH (10)
• OVE (8)
• MQP (6)
• MAX (3)
• FZT (2)
• FZX (1)
• HTF (1)
• HXX (1)
• KWP (1)
• MNI (1)

Device Packaged As Sterile

• No (41)

Sterilization Prior To Use

• Yes (41)

Issuing Agency

• GS1 (41)

Device Size Type

• 11mm (41)

Device Class

• Class I (26)
• Class II (15)

Implantable

• No (36)
• Yes (5)