Catalog Number

-

Brand Name

Single plane templates, 12 mm hole separation, 7 holes across width

Version/Model Number

AL07349001

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 19, 2019

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K023220

Product Code

JAQ

Product Code Name

System, applicator, radionuclide, remote-controlled

Public Device Record Key

3a442f92-6cb6-459c-99e0-fb3dd4c96254

Public Version Date

December 01, 2020

Public Version Number

6

DI Record Publish Date

September 19, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-