Catalog Number

7210149

Brand Name

NA

Version/Model Number

7210149

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)

Yes

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

HRX

Product Code Name

ARTHROSCOPE

Public Device Record Key

6cd29ba1-7d7a-4d01-bb8b-770b6fa9367c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 30, 2015

Package DI Number

23596010495918

Quantity per Package

6

Contains DI Package

03596010495914

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BX