Catalog Number

4600-0300

Brand Name

FIBERGRAFT BG Morsels

Version/Model Number

4600-0300

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

K151154

Product Code

MQV

Product Code Name

Filler, Bone Void, Calcium Compound

Public Device Record Key

3a2820a4-385e-492c-aedb-37c341969820

Public Version Date

June 19, 2020

Public Version Number

5

DI Record Publish Date

November 28, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-