Catalog Number

-

Brand Name

Cellfina Motor Module Device and Package

Version/Model Number

CM1 Rev G

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

K161885

Product Code

OUP

Product Code Name

Powered Surgical Instrument For Improvement In The Appearance Of Cellulite

Public Device Record Key

c403564c-062f-469c-a5b2-acb2aa79e9a1

Public Version Date

February 03, 2020

Public Version Number

1

DI Record Publish Date

January 24, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-