Duns Number:218648211
Device Description: HEADLESS CANNULATED SCREW GUIDE PIN 0.035 inches X 6 inches
Catalog Number
OS202735
Brand Name
ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS
Version/Model Number
OS202735
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K110895,K110895
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
4b01ac3c-4055-4e9d-a080-fdcd11711a8d
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
January 20, 2017
Package DI Number
05055662934533
Quantity per Package
10
Contains DI Package
05055662934540
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Cardboard Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 262 |
2 | A medical device with a moderate to high risk that requires special controls. | 1530 |