Duns Number:156567492
Catalog Number
BTA-99
Brand Name
Innovasis® Cranial System
Version/Model Number
BTA-99
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K141644
Product Code
GWO
Product Code Name
Plate, Cranioplasty, Preformed, Alterable
Public Device Record Key
1b0dc73d-6f21-4432-aae6-b3c09517e388
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
December 29, 2014
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 | 252 |
2 | A medical device with a moderate to high risk that requires special controls. | 2102 |