Catalog Number

-

Brand Name

TriPore

Version/Model Number

1105-1210

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 09, 2016

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

K070132

Product Code

MQV

Product Code Name

Filler, Bone Void, Calcium Compound

Public Device Record Key

f119128b-9d78-4e62-a2f7-adb69d6db041

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-