Catalog Number

59-23021

Brand Name

PROFYLE

Version/Model Number

59-23021

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K062498,K062498

Product Code

HRS

Product Code Name

PLATE, FIXATION, BONE

Public Device Record Key

c1ba5b8c-78bd-4c02-adc0-955634b3dabd

Public Version Date

April 06, 2022

Public Version Number

7

DI Record Publish Date

September 24, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-