Catalog Number

-

Brand Name

10mm HTR Implant System, Non-Sterile

Version/Model Number

220-10-004

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

K121008

Product Code

HTY

Product Code Name

Pin, Fixation, Smooth

Public Device Record Key

d7d6f7ba-8c25-4219-b02d-5ab22a86eab8

Public Version Date

April 06, 2022

Public Version Number

4

DI Record Publish Date

July 05, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-