Duns Number:868856969
Device Description: 5.0mmD x 6mmL, 3.4mmD Platform
Catalog Number
655006
Brand Name
InterActive® Implant
Version/Model Number
655006
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 22, 2019
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
-
Product Code
-
Product Code Name
-
Public Device Record Key
05c235d3-b64e-426a-8152-e0d1cd9f77a2
Public Version Date
August 30, 2019
Public Version Number
4
DI Record Publish Date
September 14, 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 | 328 |
2 | A medical device with a moderate to high risk that requires special controls. | 1817 |
U | Unclassified | 6 |