Catalog Number

IM1700019

Brand Name

Sequel Medical

Version/Model Number

IM1700019

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K202833

Product Code

JDW

Product Code Name

Pin, Fixation, Threaded

Public Device Record Key

a0d11d76-5033-4f36-9b78-8f9c25117eb6

Public Version Date

November 23, 2021

Public Version Number

2

DI Record Publish Date

August 16, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-