SEARCH RESULTS FOR: seaspine(2 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (2)

Brand Name

• SeaSpine Spacer System - Redondo™ (2)

GMDN Term Name

• Spinal implant trial (1)
• Vertebral body prosthesis, non-sterile (1)

GMDN Term Status

• Active (1)
• Obsolete (1)

FDA Product Code Name

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

FDA Product Code

• MAX (2)
• MQP (2)

Device Packaged As Sterile

• No (2)

Sterilization Prior To Use

• Yes (2)

Issuing Agency

• GS1 (2)

Device Size Type

• 38mm x 26mm x 20mm, 12° (2)

Device Class

• Class II (2)

Implantable

• No (2)