Duns Number:152008371
Device Description: Orthex Drill 3.5x160mm, Cannulated
Catalog Number
Z402P-160-35C
Brand Name
Orthex Drill Cannulated
Version/Model Number
Z402P-160-35C
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
K151881
Product Code
HTW
Product Code Name
Bit, Drill
Public Device Record Key
90177e49-cdfd-4d8b-b688-0bb03ee5093e
Public Version Date
November 23, 2021
Public Version Number
7
DI Record Publish Date
March 09, 2018
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 | 345 |
2 | A medical device with a moderate to high risk that requires special controls. | 540 |