Duns Number:131747628
Catalog Number
CS6016-9
Brand Name
Sonoma Orthopedic Products, Inc.
Version/Model Number
1.6mm x 9" K-Wire
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 07, 2020
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
-
Product Code
HSB
Product Code Name
Rod, Fixation, Intramedullary And Accessories
Public Device Record Key
bf2cd1cd-d365-4fb2-83ac-8e0d057a4fcf
Public Version Date
July 08, 2020
Public Version Number
3
DI Record Publish Date
November 12, 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 | 6506 |
2 | A medical device with a moderate to high risk that requires special controls. | 3411 |
3 | A medical device with high risk that requires premarket approval | 1 |
U | Unclassified | 2 |