SEARCH RESULTS FOR: seaspine(50 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (50)

Brand Name

• SeaSpine Spacer System - Pacifica™ (50)

GMDN Term Name

• Vertebral body prosthesis, non-sterile (50)

GMDN Term Status

• Obsolete (50)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (50)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (50)

FDA Product Code

• MAX (50)
• MQP (50)

Device Packaged As Sterile

• No (50)

Sterilization Prior To Use

• Yes (50)

Issuing Agency

• GS1 (50)

Device Size Type

• 9mm x 20mm x 11mm (2)
• 9mm x 20mm x 12mm (2)
• 9mm x 20mm x 13mm (2)
• 9mm x 20mm x 15mm (2)
• 9mm x 20mm x 17mm (2)
• 9mm x 20mm x 7mm (2)
• 9mm x 20mm x 8mm (2)
• 9mm x 20mm x 9mm (2)
• 9mm x 24mm x 10mm (2)
• 9mm x 24mm x 11mm (2)
• 9mm x 24mm x 12mm (2)
• 9mm x 24mm x 13mm (2)
• 9mm x 24mm x 15mm (2)
• 9mm x 24mm x 17mm (2)
• 9mm x 24mm x 9mm (2)
• 11mm x 20mm x 10mm (1)
• 11mm x 20mm x 11mm (1)
• 11mm x 20mm x 12mm (1)
• 11mm x 20mm x 13mm (1)
• 11mm x 20mm x 15mm (1)
• 11mm x 20mm x 17mm (1)
• 11mm x 20mm x 7mm (1)
• 11mm x 20mm x 8mm (1)
• 11mm x 20mm x 9mm (1)
• 11mm x 24mm x 10mm (1)
See more

Device Class

• Class II (50)

Implantable

• No (50)