SEARCH RESULTS FOR: seaspine(66 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (66)

Brand Name

• Posterior Disc Prep (66)

GMDN Term Name

• Bone curette, reusable (15)
• Bone file (11)
• Orthopaedic surgical distractor, internal (11)
• Instrument tray, reusable (10)
• Spinal rongeur (8)
• Bone file/rasp, manual, reusable (2)
• Bone graft funnel (2)
• Orthopaedic joint/limb rongeur (2)
• Surgical/emergency suction cannula, non-illuminating, reusable (2)
• Bone lever/elevator, reusable (1)
• Implant handling forceps, scissors-like (1)
• Orthopaedic graft inserter (1)

GMDN Term Status

• Active (54)
• Obsolete (12)

FDA Product Code Name

• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (17)
• CURETTE (15)
• RASP (13)
• Orthopedic tray (10)
• RONGEUR (10)
• FORCEPS (1)

FDA Product Code

• LXH (17)
• HTF (15)
• HTR (13)
• HTX (10)
• OJH (10)
• HTD (1)

Device Packaged As Sterile

• No (66)

Sterilization Prior To Use

• Yes (66)

Issuing Agency

• GS1 (66)

Device Size Type

• 8mm (6)
• 3mm (3)
• 5mm (3)
• 10mm (2)
• 11mm (2)
• 12mm (2)
• 13mm (2)
• 14mm (2)
• 15mm (2)
• 16mm (2)
• 2mm (2)
• 4mm (2)
• 6mm (2)
• 7mm (2)
• 9mm (2)

Device Class

• Class I (66)

Implantable

• No (66)