SEARCH RESULTS FOR: seaspine(41 results)

Company Name

• Seaspine Orthopedics Corporation (41)

Brand Name

• SeaSpine Spacer System - Pacifica (7)
• Shoreline ASC (6)
• Disc Prep (5)
• SeaSpine Spacer System - Hollywood™ (4)
• Cambria (2)
• PLIF Allograft (2)
• Posterior Disc Prep (2)
• Sierra (2)
• Steerable IBD (2)
• Zuma-C™ (2)
• Laminoplasty (1)
• Lateral Retractor (1)
• NewPort (1)
• RAPID Graft Delivery (1)
• Sierra™ (1)
• Vu cPOD (1)
• Zuma-C (1)

GMDN Term Name

• Orthopaedic surgical distractor, internal (9)
• Bone file (7)
• Vertebral body prosthesis, non-sterile (7)
• Spinal implant trial (5)
• Bone file/rasp, manual, reusable (4)
• Bone curette, reusable (1)
• Bone tap, reusable (1)
• Cannulated surgical drill bit, single-use (1)
• General internal orthopaedic fixation system implantation kit (1)
• Orthopaedic implant driver (1)
• Orthopaedic implantation sleeve, reusable (1)
• Orthopaedic retractor (1)
• Surgical drill guide, reusable (1)
• Surgical screwdriver, reusable (1)

GMDN Term Status

• Active (26)
• Obsolete (15)

FDA Product Code Name

• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (11)
• RASP (10)
• Intervertebral fusion device with integrated fixation, cervical (8)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (4)
• Intervertebral fusion device with bone graft, lumbar (2)
• SCREWDRIVER (2)
• APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
• CURETTE (1)
• CUTTER, SURGICAL (1)
• Guide, surgical, instrument (1)
• ORTHOSIS, SPINAL PEDICLE FIXATION (1)
• RETRACTOR (1)
• TAP, BONE (1)

FDA Product Code

• LXH (11)
• HTR (10)
• OVE (8)
• MQP (4)
• HXX (2)
• MAX (2)
• FZT (1)
• FZX (1)
• GAD (1)
• HTF (1)
• HWX (1)
• KWP (1)
• MNI (1)

Device Packaged As Sterile

• No (41)

Sterilization Prior To Use

• Yes (41)

Issuing Agency

• GS1 (41)

Device Size Type

• 7mm (41)

Device Class

• Class I (28)
• Class II (13)

Implantable

• No (41)