Duns Number:081224143
Device Description: K-Wire, .054 Blunt End, 500mm
Catalog Number
-
Brand Name
Fixcet Spinal Facet Screw System
Version/Model Number
X063-0073
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
-
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
GDF
Product Code Name
GUIDE, NEEDLE, SURGICAL
Public Device Record Key
7cbc91ba-f916-4cf0-9f9c-fa336856fe56
Public Version Date
June 03, 2021
Public Version Number
5
DI Record Publish Date
August 24, 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 | 1719 |
2 | A medical device with a moderate to high risk that requires special controls. | 3162 |
U | Unclassified | 25 |