Duns Number:687388178
Device Description: MiNi Internal Ø3.25/ L=10
Catalog Number
MIIF3310C
Brand Name
MiNi Internal Internal Fixture
Version/Model Number
MIIF3310
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
K150537
Product Code
DZE
Product Code Name
Implant, Endosseous, Root-Form
Public Device Record Key
000c7e40-7065-47c4-88eb-fe748da9e805
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
July 27, 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 | 1261 |
2 | A medical device with a moderate to high risk that requires special controls. | 3498 |