SEARCH RESULTS FOR: seaspine(23 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (23)

Brand Name

• SeaSpine Spacer System - Hollywood VI NanoMetalene (23)

GMDN Term Name

• Vertebral body prosthesis (23)

GMDN Term Status

• Active (23)

FDA Product Code Name

• Intervertebral fusion device with bone graft, cervical (23)
• Intervertebral fusion device with bone graft, lumbar (23)

FDA Product Code

• MAX (23)
• ODP (23)

Device Packaged As Sterile

• Yes (23)

Sterilization Prior To Use

• No (23)

Issuing Agency

• GS1 (23)

Device Size Type

• 11mm x 27mm x 10mm (1)
• 11mm x 27mm x 11mm (1)
• 11mm x 27mm x 12mm (1)
• 11mm x 27mm x 13mm (1)
• 11mm x 27mm x 14mm (1)
• 11mm x 27mm x 15mm (1)
• 11mm x 27mm x 16mm (1)
• 11mm x 27mm x 17mm (1)
• 11mm x 27mm x 18mm (1)
• 11mm x 27mm x 7mm (1)
• 11mm x 27mm x 8mm (1)
• 11mm x 27mm x 9mm (1)
• 11mm x 30mm x 10mm (1)
• 11mm x 30mm x 11mm (1)
• 11mm x 30mm x 12mm (1)
• 11mm x 30mm x 13mm (1)
• 11mm x 30mm x 14mm (1)
• 11mm x 30mm x 15mm (1)
• 11mm x 30mm x 16mm (1)
• 11mm x 30mm x 17mm (1)
• 11mm x 30mm x 18mm (1)
• 11mm x 30mm x 8mm (1)
• 11mm x 30mm x 9mm (1)

Device Class

• Class II (23)

Implantable

• Yes (23)