Integra® Bovine Pericardium Dural Graft - Integra® Bovine Pericardium Dural Graft is a - Integra Lifesciences Corporation

Duns Number:083171244

Device Description: Integra® Bovine Pericardium Dural Graft is a natural, resorbable, collagenous device for u Integra® Bovine Pericardium Dural Graft is a natural, resorbable, collagenous device for use in the repair of dura mater. The device is derived from bovine pericardium and is manufactured using a multistep proprietary process which gently cleans and dehydrates the tissue. The device is terminally sterilized by gamma irradiation. The device must be sutured in place.

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More Product Details

Catalog Number

BP10405

Brand Name

Integra® Bovine Pericardium Dural Graft

Version/Model Number

BP10405

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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"

-

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

K132850

Product Code Details

Product Code

GXQ

Product Code Name

DURA SUBSTITUTE

Device Record Status

Public Device Record Key

f7abdaf1-ef1f-487f-b8b7-c2db67deada9

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