Responsive Orthopedics Total Knee Arthroplasty System - TRIAL 90-SRK-160412 POLY CR 4X12MM - RESPONSIVE ORTHOPEDICS, LLC

Duns Number:080074787

Device Description: TRIAL 90-SRK-160412 POLY CR 4X12MM

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More Product Details

Catalog Number

90-SRK-160412

Brand Name

Responsive Orthopedics Total Knee Arthroplasty System

Version/Model Number

90-SRK-160412

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

JWH

Product Code Name

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Device Record Status

Public Device Record Key

099cf078-15de-4384-bcb4-3cde6a7feef5

Public Version Date

March 22, 2022

Public Version Number

5

DI Record Publish Date

September 06, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"RESPONSIVE ORTHOPEDICS, LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 476