SEARCH RESULTS FOR: seaspine(72 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (72)

Brand Name

• Cambria™ (72)

GMDN Term Name

• Vertebral body prosthesis, non-sterile (72)

GMDN Term Status

• Obsolete (72)

FDA Product Code Name

• Intervertebral fusion device with bone graft, cervical (56)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (16)

FDA Product Code

• ODP (56)
• MQP (16)

Device Packaged As Sterile

• No (72)

Sterilization Prior To Use

• Yes (72)

Issuing Agency

• GS1 (72)

Device Size Type

• 13mm x 12mm x 10mm (2)
• 13mm x 12mm x 11mm (2)
• 13mm x 12mm x 12mm (2)
• 13mm x 12mm x 5mm (2)
• 13mm x 12mm x 6mm (2)
• 13mm x 12mm x 7mm (2)
• 13mm x 12mm x 8mm (2)
• 13mm x 12mm x 9mm (2)
• 15mm x 13mm x 10mm (2)
• 15mm x 13mm x 11mm (2)
• 15mm x 13mm x 12mm (2)
• 15mm x 13mm x 5mm (2)
• 15mm x 13mm x 6mm (2)
• 15mm x 13mm x 7mm (2)
• 15mm x 13mm x 8mm (2)
• 15mm x 13mm x 9mm (2)
• 17mm x 13mm x 10mm (2)
• 17mm x 13mm x 11mm (2)
• 17mm x 13mm x 12mm (2)
• 17mm x 13mm x 5mm (2)
• 17mm x 13mm x 6mm (2)
• 17mm x 13mm x 7mm (2)
• 17mm x 13mm x 8mm (2)
• 17mm x 13mm x 9mm (2)
• 13 x 12 x 10mm (1)
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Device Class

• Class II (72)

Implantable

• No (72)