SEARCH RESULTS FOR: seaspine(3 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (3)

Brand Name

• SeaSpine Spacer System - Redondo™ (3)

GMDN Term Name

• Spinal implant trial (2)
• Vertebral body prosthesis, non-sterile (1)

GMDN Term Status

• Active (2)
• Obsolete (1)

FDA Product Code Name

• Intervertebral fusion device with bone graft, lumbar (3)
• SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (3)

FDA Product Code

• MAX (3)
• MQP (3)

Device Packaged As Sterile

• No (3)

Sterilization Prior To Use

• Yes (3)

Issuing Agency

• GS1 (3)

Device Size Type

• 38mm x 26mm x 14mm, 12° (3)

Device Class

• Class II (3)

Implantable

• No (3)