Duns Number:314546664
Device Description: The FRAXION™ Marking Sheets are used togethter with the FRAXION™ Stereotactic Frame in ord The FRAXION™ Marking Sheets are used togethter with the FRAXION™ Stereotactic Frame in order to locate the treatment target in the coordinate system and position the patient. The marking sheets will be stored together with all patient-specific parts in the storage box for the whole treatment time.
Catalog Number
P10106-200
Brand Name
Fraxion
Version/Model Number
P10106-200
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K112210,K112210
Product Code
IYE
Product Code Name
Accelerator, Linear, Medical
Public Device Record Key
d358ea0d-3094-4c37-8aaf-ebb189d609fb
Public Version Date
October 13, 2021
Public Version Number
5
DI Record Publish Date
August 23, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 175 |