Duns Number:056038268
Catalog Number
-
Brand Name
Natural Nail®
Version/Model Number
00-2490-025-34
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 16, 2017
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
-
Product Code
KIK
Product Code Name
HOOK, BONE
Public Device Record Key
da368e8f-0495-4d53-9867-b19c38124aca
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
November 30, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 8464 |
2 | A medical device with a moderate to high risk that requires special controls. | 20880 |
3 | A medical device with high risk that requires premarket approval | 133 |