CATAMARAN™ SIJ Fusion System

Basic Information

• Brand Name: CATAMARAN™ SIJ Fusion System
• Primary DI: 00850033676143
• Version / Model: 40340
• Catalog Number: 40340
• Company Name: TENON MEDICAL, INC.
• Labeler DUNS: 117014636
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2021-12-17
• Public Version: 1
• Public Version Date: 2021-12-27
• Public Version Status: New
• Public Device Record Key: 6b1431f4-2307-4a0a-a7cb-e017d0a6d22c

Device Description

Funnel Tube 10mm, Catamaran

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
OUR	Sacroiliac Joint Fixation	Orthopedic	888.3040	2

GMDN Terms

Code	Name	Definition	Implantable	Status
62399	Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated, non-sterile	A non-sterile implantable device designed to be inserted across the sacroiliac joint to provide temporary stabilization and to encourage long-term joint fusion, typically to alleviate pain from the joint. It is made of uncoated metal [e.g., titanium (Ti)], and typically in the form of a cylinder which may be threaded and/or fenestrated. It is typically surgically implanted under fluoroscopic guidance and may include dedicated disposable implantation instruments.	No	Obsolete

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00850033676143	GS1

Premarket Submissions

Submission Number	Supplement Number
K180818	000