Duns Number:183641617
Device Description: DILATION TUBE 3
Catalog Number
117-318
Brand Name
Avatar 2.0
Version/Model Number
117-318
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
K111953
Product Code
NKB
Product Code Name
Thoracolumbosacral pedicle screw system
Public Device Record Key
53824093-4cbd-41c0-b4e8-7a09de559eb0
Public Version Date
November 14, 2019
Public Version Number
1
DI Record Publish Date
November 06, 2019
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 | 315 |
2 | A medical device with a moderate to high risk that requires special controls. | 9180 |
U | Unclassified | 47 |