Duns Number:081067703
Catalog Number
NBF1-50X10-01
Brand Name
NexGraft
Version/Model Number
NBF1-50X10-01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 05, 2016
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
K092046
Product Code
MQV
Product Code Name
Filler, Bone Void, Calcium Compound
Public Device Record Key
43768ce5-096e-4929-ba94-f2431de8e5ba
Public Version Date
October 19, 2020
Public Version Number
5
DI Record Publish Date
April 08, 2016
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 178 |