FDA.reportPublic FDA data

Fraxion

Primary DI
04056719001643
Brand
Fraxion
Company
3C-Medical Intelligence GmbH
Model
P10106-602
Catalog number
P10106-602
Device description
"""The Fraxion FRAXION™ Kit includes all necessary components to generate a patient-specific mouthpiece. It contains also the necessary Saliva Stop Patient which prevents salivafrom reaching the Patient Control Unit (sufficient for up to 20 patients)."""
Published
2016-08-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
IYEAccelerator, Linear, Medical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
IYEAccelerator, Linear, MedicalRadiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K112210000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K112210000FRAXIONMedical Intelligence Medizintechnik GmbH2011-11-22IYE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04056719001643PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04056719001643040567190016434056719001643

GMDN Terms#

Term, Definition table
TermDefinition
Stereotactic radiosurgical/radiotherapy arch head frameA 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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
314546664
Device count
1
DM exempt
true
Kit
true
Lot or batch
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04056719002268iGUIDEP10603-111-224P10603-1112026-04-22
04056719002190iGUIDEP10603-111-223P10603-1112019-08-01
04056719001704iGUIDEP10603-109P10603-1092016-08-23
04056719001742iGUIDEP10603-110P10603-1102017-02-24
04056719002039iGUIDEP10603-111P10603-1112017-10-13
04056719001728BodyFIXP10102-305 P10102-305 2016-08-23
04056719001735BodyFIXP10102-309P10102-3092016-08-23
04056719001773FraxionP10106-322 P10106-322 2016-08-23
04056719001780FraxionP10106-323 P10106-323 2016-08-23
04056719001803HeadFIXP10103-309 P10103-309 2016-08-23
04056719001810HeadFIXP10103-311 P10103-311 2016-08-23
04056719001827HeadFIXP10103-312 P10103-312 2016-08-23
04056719001834HeadFIXP10103-403 P10103-403 2016-08-23
04056719001858HeadFIXP10103-603 P10103-603 2016-08-23
04056719001865HeadFIXP10103-604 P10103-604 2016-08-23
04056719002220iBEAM®P10105-1822020-06-18
04056719002251iBEAMP10105-184P10105-1842022-07-12
04056719002244HexaPODP10603-300P10603-3002021-09-28
04056719002213iBEAM®P10105-3002020-08-20
04056719002237iBEAM®P10105-1832020-07-07

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Primary DI, Brand, Company table
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