Duns Number:534128491
Device Description: Anti-rotation Abutment, 3 mm Diameter, 12 mm lengh
Catalog Number
P3-3,12
Brand Name
Prosthetic Accessories
Version/Model Number
P3-3,12
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
K112440,K112440
Product Code
NHA
Product Code Name
Abutment, Implant, Dental, Endosseous
Public Device Record Key
bf0c9f93-cd7a-435b-9cef-5dabf320996c
Public Version Date
May 13, 2019
Public Version Number
1
DI Record Publish Date
May 05, 2019
Package DI Number
17290111272803
Quantity per Package
10
Contains DI Package
07290111272806
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Bag
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 190 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 276 |