Duns Number:315018218
Device Description: CRANIOPLATE 1.5 2HOLES STR.L:11MM
Catalog Number
FM960T
Brand Name
CRANIOPLATE
Version/Model Number
FM960T
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 25, 2021
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
Yes
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
-
Product Code
JEY
Product Code Name
PLATE, BONE
Public Device Record Key
7e79e129-cb7b-480a-9661-53a8ff111d79
Public Version Date
March 27, 2019
Public Version Number
3
DI Record Publish Date
September 30, 2015
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 11840 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7088 |
| 3 | A medical device with high risk that requires premarket approval | 37 |