Catalog Number

102-99-45

Brand Name

Flow-Screw™

Version/Model Number

102-99-45

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

-

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

K142776

Product Code

LRP

Product Code Name

Tray, Surgical

Public Device Record Key

d0e6678e-c2ea-4a7c-b7f3-795e6212a4d3

Public Version Date

September 16, 2022

Public Version Number

2

DI Record Publish Date

February 08, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-