SEARCH RESULTS FOR: seaspine(2 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (2)

Brand Name

• SeaSpine Spacer System - Hollywood NanoMetalene (1)
• SeaSpine Spacer System - Hollywood™ (1)

GMDN Term Name

• Vertebral body prosthesis, non-sterile (2)

GMDN Term Status

• Obsolete (2)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (2)
• Intervertebral fusion device with bone graft, cervical (1)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (1)

FDA Product Code

• MAX (2)
• MQP (1)
• ODP (1)

Device Packaged As Sterile

• No (2)

Sterilization Prior To Use

• Yes (2)

Issuing Agency

• GS1 (2)

Device Size Type

• 11mm x 30mm x 11mm (2)

Device Class

• Class II (2)

Implantable

• No (2)