Duns Number:534128491
Device Description: Angular Adaptor Single Unit
Catalog Number
P64-3.75,17-0.5
Brand Name
Prosthetic Accessories
Version/Model Number
P64-3.75,17-0.5
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
K182455,K182455
Product Code
NHA
Product Code Name
Abutment, Implant, Dental, Endosseous
Public Device Record Key
93955885-d0d6-4861-8cc8-87e86de4b556
Public Version Date
October 07, 2019
Public Version Number
1
DI Record Publish Date
September 29, 2019
Package DI Number
17290111273909
Quantity per Package
10
Contains DI Package
07290111273902
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 |