Timberline Lateral Fusion System

Basic Information

• Brand Name: Timberline Lateral Fusion System
• Primary DI: 03662663274333
• Version / Model: 8735-3002
• Catalog Number: 8735-3002
• Company Name: Highridge Medical, LLC
• Labeler DUNS: 119260394
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2025-12-18
• Public Version: 1
• Public Version Date: 2025-12-26
• Public Version Status: New
• Public Device Record Key: 48226111-d648-4941-8d5b-539e3ec0f78e

Device Description

SENTIO NAVIGATION PROBE STER

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• 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: Yes
• Has Serial Number: No
• Has Lot/Batch Number: No
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
HXB	PROBE	Orthopedic	888.4540	1

GMDN Terms

Code	Name	Definition	Implantable	Status
47862	Abdominal/ENT/orthopaedic surgical probe, reusable	A slender, rod-like, hand-held manual surgical instrument intended to be used to explore cavities, wounds or fistulas during abdominal, ENT, and/or orthopaedic surgical interventions; it does not include stereotactic devices and is not dedicated to endoscopy. It may have a blunt bulbous, paddle-like, or pointed tip, may be single- or double-ended, and the shaft may be straight, bent or hooked. It is made of rigid or flexible metallic and/or synthetic polymer material. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	03662663274333	GS1

Customer Contacts

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