Duns Number:010968002
Device Description: 7.0 Screw Countersink
Catalog Number
009-000048
Brand Name
Headed Screw System Instruments
Version/Model Number
009-000048
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
MRI safety Status
MR Conditional
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
HWW
Product Code Name
COUNTERSINK
Public Device Record Key
804ccc6b-b315-45d5-9139-2ac2e3341690
Public Version Date
September 02, 2019
Public Version Number
1
DI Record Publish Date
August 23, 2019
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 | 440 |
2 | A medical device with a moderate to high risk that requires special controls. | 7793 |