Rheo Knee - RHEO KNEE 3 Trials - OSSUR AMERICAS, INC.

Duns Number:139280028

Device Description: RHEO KNEE 3 Trials

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More Product Details

Catalog Number

RKN130203

Brand Name

Rheo Knee

Version/Model Number

RKN130203

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 28, 2020

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

ISW

Product Code Name

ASSEMBLY, KNEE/SHANK/ANKLE/FOOT, EXTERNAL

Device Record Status

Public Device Record Key

3c10ad8e-c86b-42e0-983d-284f30edabc6

Public Version Date

March 09, 2021

Public Version Number

2

DI Record Publish Date

May 16, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"OSSUR AMERICAS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 251