Duns Number:006261481
Device Description: BAND 670100 SIMPLICI-T ANNULOPLASTY 10L
Catalog Number
-
Brand Name
SIMPLICI-T®
Version/Model Number
670100
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
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
K052970
Product Code
KRH
Product Code Name
RING, ANNULOPLASTY
Public Device Record Key
23157428-f3d2-4659-b4f4-47ba2d7ec940
Public Version Date
February 05, 2021
Public Version Number
2
DI Record Publish Date
September 06, 2020
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 | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |