Duns Number:317409001
Catalog Number
OC06D.067.032 STE
Brand Name
GUIDE PIN & GUIDE SCREW SET
Version/Model Number
OC06D.067.032
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
K131264,K131264
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
7b5e3b13-a979-40c0-8c79-8fbbcebc6d4f
Public Version Date
March 09, 2021
Public Version Number
1
DI Record Publish Date
March 01, 2021
Package DI Number
24053613284374
Quantity per Package
1
Contains DI Package
14053613284377
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 154 |
2 | A medical device with a moderate to high risk that requires special controls. | 70 |