Duns Number:078818942
Catalog Number
-
Brand Name
Montage Fast Set
Version/Model Number
OS-MON-1001FS
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"
Yes
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MTJ
Product Code Name
Wax, Bone
Public Device Record Key
8e4fac34-2807-42b9-a6f6-7fb1de7b6610
Public Version Date
February 22, 2021
Public Version Number
1
DI Record Publish Date
February 12, 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 |
---|---|---|
U | Unclassified | 20 |