Catalog Number

-

Brand Name

ForceFlex

Version/Model Number

SS655

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

PTX

Product Code Name

Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, Exempt

Public Device Record Key

3f93f004-6b31-4ff2-9334-5cafa3169679

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

June 16, 2020

Package DI Number

10810020083559

Quantity per Package

12

Contains DI Package

00810020083552

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-