Catalog Number

AR-2324BCM-1

Brand Name

Arthrex®

Version/Model Number

AR-2324BCM-1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

5f695178-7f15-464c-b8d8-3255b06aa04c

Public Version Date

October 10, 2019

Public Version Number

6

DI Record Publish Date

November 30, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-