Catalog Number

-

Brand Name

Smith and Nephew

Version/Model Number

72203519

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K172092

Product Code

HRX

Product Code Name

Arthroscope

Public Device Record Key

89d1aed5-4a24-4251-a480-b49b28724f5b

Public Version Date

July 04, 2022

Public Version Number

3

DI Record Publish Date

November 05, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-