Duns Number:080028759
Device Description: ActaStim-S Spine Fusion Stimulator System
Catalog Number
1101-0000
Brand Name
ActaStim-S
Version/Model Number
1101-0000
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
-
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
P190030
Product Code
LOF
Product Code Name
Stimulator, Bone Growth, Non-Invasive
Public Device Record Key
278a6fef-28f9-480b-af88-64c7eb7fdaf7
Public Version Date
February 16, 2021
Public Version Number
1
DI Record Publish Date
February 08, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 15 |
3 | A medical device with high risk that requires premarket approval | 11 |