DuraGen Plus™ Spinal Matrix - DuraGen Plus Dural Regeneration Matrix- Spinal - Integra Lifesciences Corporation

Duns Number:083171244

Device Description: DuraGen Plus Dural Regeneration Matrix- Spinal Matrix is an absorbable implant for repair DuraGen Plus Dural Regeneration Matrix- Spinal Matrix is an absorbable implant for repair of dural defects. DuraGen Plus Dural Regeneration Matrix-Spinal Matrix is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix. DuraGen Plus Dural Regeneration Matrix-Spinal Matrix is two 1 inch x 3 inch (2.5cm x 7.5xm) dural regeneration matrices supplied sterile, non-pyrogenic, for single use in double peel packages.

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More Product Details

Catalog Number

51100213

Brand Name

DuraGen Plus™ Spinal Matrix

Version/Model Number

51100213

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 24, 2015

Issuing Agency

In GS1

Product Characteristics

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"

Yes

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

K092388,K092388

Product Code Details

Product Code

GXQ

Product Code Name

DURA SUBSTITUTE

Device Record Status

Public Device Record Key

7fc71b32-47dd-4305-a16c-09e5b49fca8a

Public Version Date

September 22, 2020

Public Version Number

5

DI Record Publish Date

September 22, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INTEGRA LIFESCIENCES CORPORATION" Characteristics
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