EVOLUTION® - EVOLUTION® FEMORAL FINISH IMPACTOR REPLACEMENT - Microport Orthopedics Inc.

Duns Number:079118736

Device Description: EVOLUTION® FEMORAL FINISH IMPACTOR REPLACEMENT HEAD

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More Product Details

Catalog Number

E1005102CN

Brand Name

EVOLUTION®

Version/Model Number

E1005102CN

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

HWA

Product Code Name

IMPACTOR

Device Record Status

Public Device Record Key

1be0a977-319c-4ada-a300-2fcc39bc1a20

Public Version Date

June 05, 2020

Public Version Number

1

DI Record Publish Date

May 28, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MICROPORT ORTHOPEDICS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7823
2 A medical device with a moderate to high risk that requires special controls. 12222
3 A medical device with high risk that requires premarket approval 109