Duns Number:083171244
Device Description: DuraGen Plus™ Dural Regeneration Matrix is an absorbable implant for repair of dural defec DuraGen Plus™ Dural Regeneration Matrix is an absorbable implant for repair of dural defects. DuraGen Plus™ is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix. DuraGen Plus™ is supplied sterile, nonpyrogenic, for single use in double peel packages in a variety of sizes.
Catalog Number
DP5022
Brand Name
DuraGen Plus™ Dural Regeneration Matrix
Version/Model Number
DP5022
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
K032693,K032693
Product Code
GXQ
Product Code Name
DURA SUBSTITUTE
Public Device Record Key
709ba44e-c344-4b0d-863d-7192b9117c32
Public Version Date
October 04, 2022
Public Version Number
6
DI Record Publish Date
September 22, 2015
Package DI Number
30381780070935
Quantity per Package
5
Contains DI Package
10381780070931
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 14 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 75 |
| 3 | A medical device with high risk that requires premarket approval | 17 |
| U | Unclassified | 32 |