Catalog Number

A-6611

Brand Name

APTUS

Version/Model Number

A-6611

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

-

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

K193633

Product Code

HRS

Product Code Name

Plate, fixation, bone

Public Device Record Key

346003d3-d56e-44ee-b00f-d686f0089534

Public Version Date

July 08, 2021

Public Version Number

2

DI Record Publish Date

June 14, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-