Sage Cervical Interbody Fusion System

Basic Information

• Brand Name: Sage Cervical Interbody Fusion System
• Primary DI: B648C2055000
• Version / Model: C205-500
• Company Name: CURITEVA, INC.
• Labeler DUNS: 074575332
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2024-01-03
• Public Version: 1
• Public Version Date: 2024-01-11
• Public Version Status: New
• Public Device Record Key: cb40ca5e-2393-4bbc-8960-258be8bd5323

Device Description

Parallel Rasp, 5mm (12 X 11mm and 16 X 13mm Footprints)

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
ODP	Intervertebral Fusion Device With Bone Graft, Cervical	Orthopedic	888.3080	2

GMDN Terms

Code	Name	Definition	Implantable	Status
64557	Orthopaedic fixation plate file/rasp	A hand-held manual instrument designed to blunt and smooth the sharp edges of an orthopaedic fixation plate that has been cut by the surgeon during orthopaedic surgery. It is made of metal materials and is in the form of a rod with an abrasive working end, typically coated with diamond particles. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	B648C2055000	HIBCC

Customer Contacts

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

Premarket Submissions

Submission Number	Supplement Number
K181261	000

Device Sizes

Type	Value	Unit	Text
Height	5	Millimeter