Duns Number:826499238
Device Description: PLATE, L1 MMF FIXATION, 2.0 MM L1 MMF SCREW, CP TITANIUM
Catalog Number
-
Brand Name
LEVEL ONE CMF
Version/Model Number
25-197-07-09
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
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
4585b4f7-c41c-4641-b293-95e77f5e1e14
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
March 29, 2018
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 | 7013 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4618 |