Duns Number:135057938
Device Description: Simon Nitinol Filter™ , Vena Cava Filter, Femoral Introducer Set
Catalog Number
3120F
Brand Name
Simon Nitinol Filter™
Version/Model Number
3120F
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K970099
Product Code
DTK
Product Code Name
FILTER, INTRAVASCULAR, CARDIOVASCULAR
Public Device Record Key
d302fe04-1760-42a6-aaf0-00e13252c219
Public Version Date
November 02, 2020
Public Version Number
3
DI Record Publish Date
October 02, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 35 |
2 | A medical device with a moderate to high risk that requires special controls. | 2835 |
3 | A medical device with high risk that requires premarket approval | 190 |