SEARCH RESULTS FOR: seaspine(22 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (22)

Brand Name

• Disc Prep (5)
• NewPort (3)
• Posterior Disc Prep (3)
• Cambria (2)
• Laminoplasty (2)
• SeaSpine Spacer System - Hollywood (2)
• Lateral Retractor (1)
• Regatta Lateral System (1)
• UCR (1)
• Vu cPOD (1)
• Zuma-L (1)

GMDN Term Name

• Spinal rongeur (10)
• Bone file/rasp, manual, reusable (3)
• Surgical instrument handle, non-torque-limiting (3)
• Orthopaedic implant driver (2)
• Orthopaedic joint/limb rongeur (2)
• Orthopaedic implantation sleeve, reusable (1)
• Orthopaedic inorganic implant inserter/extractor, reusable (1)

GMDN Term Status

• Active (22)

FDA Product Code Name

• RONGEUR (9)
• FORCEPS (3)
• ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (3)
• RASP (3)
• RETRACTOR (2)
• SCREWDRIVER (2)

FDA Product Code

• HTX (9)
• HTD (3)
• HTR (3)
• LXH (3)
• GAD (2)
• HXX (2)

Device Packaged As Sterile

• No (22)

Sterilization Prior To Use

• Yes (22)

Issuing Agency

• GS1 (22)

Device Size Type

• 5mm (22)

Device Class

• Class I (22)

Implantable

• No (22)