SEARCH RESULTS FOR: seaspine(2 results)

Company Name

• SEASPINE ORTHOPEDICS CORPORATION (2)

Brand Name

• Posterior Disc Prep (2)

GMDN Term Name

• Bone curette, reusable (2)

GMDN Term Status

• Active (2)

FDA Product Code Name

• CURETTE (2)

FDA Product Code

• HTF (2)

Device Packaged As Sterile

• No (2)

Sterilization Prior To Use

• Yes (2)

Issuing Agency

• GS1 (2)

Device Size Type

• 8mm (2)

Device Class

• Class I (2)

Implantable

• No (2)