VERASENSE - ORTHOSENSOR INC

Duns Number:005788130

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More Product Details

Catalog Number

SNN-LGNPS78

Brand Name

VERASENSE

Version/Model Number

VERASENSE for Smith & Nephew Legion PS size 7-8

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 31, 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

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

K150372

Product Code Details

Product Code

ONN

Product Code Name

Intraoperative Orthopedic Joint Assessment Aid

Device Record Status

Public Device Record Key

f82b8977-9cff-429e-8220-0205e1e215c1

Public Version Date

January 08, 2021

Public Version Number

1

DI Record Publish Date

December 31, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ORTHOSENSOR 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. 171