Catalog Number

-

Brand Name

Solitaire™ X

Version/Model Number

SFR4-6-20-10

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

K181807,K183022

Product Code

NRY

Product Code Name

CATHETER, THROMBUS RETRIEVER

Public Device Record Key

8cfaa0d4-7e04-45a3-b61b-3d9add4328f2

Public Version Date

August 05, 2022

Public Version Number

2

DI Record Publish Date

April 29, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-