NuVasive® CoRoent® Small Interlock System. Catalog #6791714

CataBlog
Jul 17, 2022
1 min read

Vendor/Manufacturer: NuVasive®

Product/Product Line: CoRoent® Small Interlock System

Vendor/Manufacturer Catalog #: 6791714

Global Unique Device (GUD) Primary Device Identifier Number: 00887517362414

Global Unique Device (GUD) Device Description:

CoRoent® SI Screw, 4x14mm Self-Tap

Global Medical Device Nomenclature (GMDN) Preferred Term Name:

Spinal bone screw, non-bioabsorbable

Global Medical Device Nomenclature (GMDN) Definition:

A small, threaded rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a stabilization device (e.g., rod, plate) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.

FDA Regulation Medical Specialty:

Orthopedic Devices - Prosthetic Devices

FDA Regulation Number: 888.3080

FDA Regulation Description Classification Name:

Intervertebral body fusion device

FDA Classification Product Code(s): ODP

FDA Classification Product Code Device Name(s):

Intervertebral Fusion Device With Bone Graft, Cervical

FDA Premarket Submission(s): K081611 , K192582 , K102547

The NuVasive® CoRoent® Small Interlock System is

SUBSTANTIALLY EQUIVALENT to the following product(s):

1. Centinel Spine STALIF C System