SEARCH RESULTS FOR: seaspine(100 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (100)

Brand Name

• SeaSpine Spacer System - Pacifica™ (100)

GMDN Term Name

• Spinal implant trial (50)
• Vertebral body prosthesis, non-sterile (50)

GMDN Term Status

• Active (50)
• Obsolete (50)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (100)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (100)

FDA Product Code

• MAX (100)
• MQP (100)

Device Packaged As Sterile

• No (100)

Sterilization Prior To Use

• Yes (100)

Issuing Agency

• GS1 (100)

Device Size Type

• 9mm x 20mm x 11mm (4)
• 9mm x 20mm x 12mm (4)
• 9mm x 20mm x 13mm (4)
• 9mm x 20mm x 15mm (4)
• 9mm x 20mm x 17mm (4)
• 9mm x 20mm x 8mm (4)
• 9mm x 20mm x 9mm (4)
• 9mm x 24mm x 10mm (4)
• 9mm x 24mm x 11mm (4)
• 9mm x 24mm x 12mm (4)
• 9mm x 24mm x 13mm (4)
• 9mm x 24mm x 15mm (4)
• 9mm x 24mm x 17mm (4)
• 9mm x 24mm x 9mm (4)
• 9mm x 20mm x 10mm (3)
• 9mm x 20mm x 7mm (3)
• 11mm x 20mm x 10mm (2)
• 11mm x 20mm x 11mm (2)
• 11mm x 20mm x 12mm (2)
• 11mm x 20mm x 13mm (2)
• 11mm x 20mm x 15mm (2)
• 11mm x 20mm x 17mm (2)
• 11mm x 20mm x 7mm (2)
• 11mm x 20mm x 8mm (2)
• 11mm x 20mm x 9mm (2)
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Device Class

• Class II (100)

Implantable

• No (100)