Duns Number:144666109
Device Description: Plate, Large
Catalog Number
9A0P-2A12
Brand Name
PINIT PLATE®
Version/Model Number
9A0P-2A12
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K122334
Product Code
HRS
Product Code Name
Plate, Fixation, Bone
Public Device Record Key
4ad5c668-7154-4ee5-adb8-ba20c9caf02a
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
October 05, 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 | 26 |
2 | A medical device with a moderate to high risk that requires special controls. | 382 |
U | Unclassified | 7 |