Catalog Number

-

Brand Name

PROGENIX® PUTTY and PROGENIX® PLUS

Version/Model Number

006010

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)

Yes

FDA Premarket Submission

K081950

Product Code

NUN

Product Code Name

BONE GRAFTING MATERIAL, HUMAN SOURCE

Public Device Record Key

48a86f7f-90c5-4ba0-98be-f6e5b9b06485

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 20, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-