Catalog Number

-

Brand Name

HUNTER

Version/Model Number

ATBC2040

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 29, 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

-

Product Code

HXA

Product Code Name

PROSTHESIS, TENDON, PASSIVE

Public Device Record Key

8af109f4-464e-47d2-8d70-524b79543305

Public Version Date

September 23, 2019

Public Version Number

3

DI Record Publish Date

October 15, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-