Catalog Number

484008100

Brand Name

EMPHASYS

Version/Model Number

4840-08-100

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

QBO

Product Code Name

Instruments designed for press-fit osteochondral implants

Public Device Record Key

c920e4a3-66ba-4efc-aaf1-741c08134ba3

Public Version Date

September 06, 2021

Public Version Number

1

DI Record Publish Date

August 28, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-