Straumann Xenograft - Straumann Xenograft bone grafting material is a - Nibec Co., Ltd.

Duns Number:687796909

Device Description: Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produc Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

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More Product Details

Catalog Number

-

Brand Name

Straumann Xenograft

Version/Model Number

S1-0210-100

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

K113246

Product Code Details

Product Code

NPM

Product Code Name

Bone Grafting Material, Animal Source

Device Record Status

Public Device Record Key

a7b0e9f9-42b0-4aca-99c6-a684793004c3

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NIBEC CO., LTD." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 102