Fraxion

Basic Information

• Brand Name: Fraxion
• Primary DI: 04056719001544
• Version / Model: P10106-212
• Catalog Number: P10106-212
• Company Name: 3C-Medical Intelligence GmbH
• Labeler DUNS: 314546664
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2016-08-23
• Public Version: 7
• Public Version Date: 2023-12-15
• Public Version Status: Update
• Public Device Record Key: 5cbc3520-751b-4752-a9fa-a44e83b0925b

Device Description

The FRAXION™ Vacuum cushions are formed to the patients head and enable highly accurate patient repositioning. Each cushion will be moulded individually for each patient and will be stored together with all patient-specific parts in the storage box for the whole treatment time.

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: Yes
• Has Lot/Batch Number: No
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
IYE	Accelerator, Linear, Medical	Radiology	892.5050	2

GMDN Terms

Code	Name	Definition	Implantable	Status
61128	Stereotactic radiosurgical/radiotherapy arch head frame	A non-sterile device intended to be used to position and immobilize a patient’s head for reproducible positioning during radiation treatment planning, stereotactic radiotherapy (SRT), and stereotactic radiosurgery (SRS), on all parts of the brain, head, and neck. It is in the form of an arched frame to which can be attached various components (e.g., mouthpiece, nasion cushion) that non-invasively contact the patient to serve as points of reference, and which is typically attached to a base plate, couch top, or overlay. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	04056719001544	GS1

Premarket Submissions

Submission Number	Supplement Number
K112210	000