Duns Number:945385862
Device Description: Fortify Flowable Extracellular Matrix
Catalog Number
FFM-01-KIT-S
Brand Name
Fortify Flowable
Version/Model Number
G59091
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K160136
Product Code
KGN
Product Code Name
Dressing, wound, collagen
Public Device Record Key
9ce12490-766e-4caf-b716-bd5d2959c0cd
Public Version Date
August 10, 2021
Public Version Number
1
DI Record Publish Date
August 02, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 2 |
2 | A medical device with a moderate to high risk that requires special controls. | 116 |
U | Unclassified | 36 |