SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE SIZE 2 LEFT - SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE - Howmedica Osteonics Corp.

Duns Number:058311945

Device Description: SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE SIZE 2 LEFT

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More Product Details

Catalog Number

I-K4275TGL2

Brand Name

SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE SIZE 2 LEFT

Version/Model Number

I-K4275TGL2

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

HRY

Product Code Name

PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

Device Record Status

Public Device Record Key

ffd3125e-01e6-436f-98dd-e4069dd252dc

Public Version Date

March 22, 2022

Public Version Number

2

DI Record Publish Date

February 21, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HOWMEDICA OSTEONICS CORP." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 5091
2 A medical device with a moderate to high risk that requires special controls. 10216
3 A medical device with high risk that requires premarket approval 32