Duns Number:481999654
Device Description: BONE SCREWS, CROSS-FIT, SELF-TAPPING
Catalog Number
59-17022
Brand Name
PROFYLE
Version/Model Number
59-17022
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
K062498,K062498
Product Code
HRS
Product Code Name
PLATE, FIXATION, BONE
Public Device Record Key
2f9ffba2-2594-4d64-9537-1b79eb32c170
Public Version Date
January 26, 2022
Public Version Number
6
DI Record Publish Date
September 24, 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 | 2606 |
2 | A medical device with a moderate to high risk that requires special controls. | 9953 |
3 | A medical device with high risk that requires premarket approval | 186 |