Duns Number:081224143
Device Description: SPECIALTY CERTEX REDUCER ASSEMBLY
Catalog Number
-
Brand Name
Certex Spinal Fixation System
Version/Model Number
C067-0035
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
HWB
Product Code Name
EXTRACTOR
Public Device Record Key
fec12fa9-38cc-4dbb-af69-26fe51927f18
Public Version Date
June 03, 2021
Public Version Number
4
DI Record Publish Date
March 29, 2016
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 |