CoRoent

Basic Information

• Brand Name: CoRoent
• Primary DI: 00887517567239
• Version / Model: 5169280
• Company Name: Nuvasive, Inc.
• Labeler DUNS: 053950783
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2015-10-24
• Public Version: 7
• Public Version Date: 2025-07-14
• Public Version Status: Update
• Public Device Record Key: 959d5a5c-ffa8-4f73-bcbd-60da5473594c

Device Description

CoRoent Ant TLIF PEEK, 16x9x28mm 0°

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Moist Heat or Steam Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
MAX	Intervertebral fusion device with bone graft, lumbar	Orthopedic	888.3080	2
MQP	SPINAL VERTEBRAL BODY REPLACEMENT DEVICE	Orthopedic	888.3060	2
ODP	Intervertebral fusion device with bone graft, cervical	Orthopedic	888.3080	2
OVE	Intervertebral fusion device with integrated fixation, cervical	Orthopedic	888.3080	2
PHM	Intervertebral fusion device with bone graft, thoracic	Orthopedic	888.3080	2

GMDN Terms

Code	Name	Definition	Implantable	Status
38161	Metallic spinal interbody fusion cage	A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.	Yes	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00887517567239	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Premarket Submissions

Submission Number	Supplement Number
K071795	000
K081611	000
K140659	000
K141665	000
K150994	000
K151472	000
K153419	000
K161230	000
K170961	000
K231735	000