Catalog Number

-

Brand Name

PATTERSON

Version/Model Number

089-9674

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

Product Code

GAT

Product Code Name

Suture, Nonabsorbable, Synthetic, Polyethylene

Public Device Record Key

d2b4ee1d-eea5-4e5a-be95-445d43fa0e11

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 25, 2015

Package DI Number

D6620708996742

Quantity per Package

12

Contains DI Package

D6620708996740

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box