Catalog Number

AR-2324KPSLC

Brand Name

Arthrex®

Version/Model Number

AR-2324KPSLC

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

-

Product Code

MAI

Product Code Name

Fastener, fixation, biodegradable, soft tissue

Public Device Record Key

1a6e4390-2df5-443a-9441-95e05c380dce

Public Version Date

March 24, 2020

Public Version Number

1

DI Record Publish Date

March 16, 2020

Package DI Number

10888867351339

Quantity per Package

5

Contains DI Package

00888867351332

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box