Catalog Number

AR-7268T

Brand Name

Arthrex®

Version/Model Number

AR-7268T

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

GAT

Product Code Name

SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Public Device Record Key

d1e2c0ce-4c43-4c50-909e-7353d1b18d01

Public Version Date

September 08, 2022

Public Version Number

2

DI Record Publish Date

March 08, 2021

Package DI Number

10888867369907

Quantity per Package

5

Contains DI Package

00888867369900

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box