Duns Number:332192830
Device Description: 1000-2000 µm; 5 x 1.0 ml
Catalog Number
KE 19010510
Brand Name
BioResorb® Macro Pore
Version/Model Number
KE 19010510
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
K050260
Product Code
LYC
Product Code Name
Bone Grafting Material, Synthetic
Public Device Record Key
25d7679a-deb0-425e-9714-24faea62b0e9
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 25, 2015
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. | 16 |