Catalog Number

59000200

Brand Name

FIBERGRAFT Aeridyan Matrix

Version/Model Number

59000200

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

K182670

Product Code

MQV

Product Code Name

Filler, Bone Void, Calcium Compound

Public Device Record Key

ecc9635d-a1f9-43ef-a8c4-f6a4615ca1dd

Public Version Date

August 12, 2021

Public Version Number

1

DI Record Publish Date

August 04, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-