Catalog Number

006-AGL

Brand Name

Agilon

Version/Model Number

006-AGL

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

K190371,K193168

Product Code

MQV

Product Code Name

Filler, Bone Void, Calcium Compound

Public Device Record Key

dfe18ea3-6d4f-4fda-ac8a-7070c596cb0e

Public Version Date

February 04, 2021

Public Version Number

4

DI Record Publish Date

August 21, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-