Catalog Number

5099050

Brand Name

NuOss DS

Version/Model Number

5099050

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

K170541

Product Code

NPM

Product Code Name

BONE GRAFTING MATERIAL, ANIMAL SOURCE

Public Device Record Key

65ed26f0-ab5b-42f1-9d7b-d00f08b8d075

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 19, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-