Revolution - Cement Mixing System with MIS Femoral Breakaway - STRYKER CORPORATION

Duns Number:196548481

Device Description: Cement Mixing System with MIS Femoral Breakaway Nozzle and Advanced Femoral Canal Pressuri Cement Mixing System with MIS Femoral Breakaway Nozzle and Advanced Femoral Canal Pressurizer (Medium)

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More Product Details

Catalog Number

0606-595-000

Brand Name

Revolution

Version/Model Number

0606595000

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

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

-

Product Code Details

Product Code

JDZ

Product Code Name

MIXER, CEMENT, FOR CLINICAL USE

Device Record Status

Public Device Record Key

afcc1726-1551-4e39-9fbb-6026b3c6eb85

Public Version Date

March 22, 2021

Public Version Number

2

DI Record Publish Date

September 24, 2018

Additional Identifiers

Package DI Number

37613154169697

Quantity per Package

6

Contains DI Package

07613154169696

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack

"STRYKER CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2188
2 A medical device with a moderate to high risk that requires special controls. 3183
U Unclassified 60