SEARCH RESULTS FOR: seaspine(9 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (9)

Brand Name

• Cambria™ (8)
• Cambria (1)

GMDN Term Name

• Spinal implant trial (6)
• Vertebral body prosthesis, non-sterile (2)
• Bone file/rasp, manual, reusable (1)

GMDN Term Status

• Active (7)
• Obsolete (2)

FDA Product Code Name

• Intervertebral fusion device with bone graft, cervical (4)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (4)
• RASP (1)

FDA Product Code

• MQP (4)
• ODP (4)
• HTR (1)

Device Packaged As Sterile

• No (9)

Sterilization Prior To Use

• Yes (9)

Issuing Agency

• GS1 (9)

Device Size Type

• 13mm x 12mm x 11mm (9)

Device Class

• Class II (8)
• Class I (1)

Implantable

• No (9)