Duns Number:139280028
Device Description: RHEO KNEE 3 Trials
Catalog Number
RKN130203
Brand Name
Rheo Knee
Version/Model Number
RKN130203
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 28, 2020
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
-
Product Code
ISW
Product Code Name
ASSEMBLY, KNEE/SHANK/ANKLE/FOOT, EXTERNAL
Public Device Record Key
3c10ad8e-c86b-42e0-983d-284f30edabc6
Public Version Date
March 09, 2021
Public Version Number
2
DI Record Publish Date
May 16, 2018
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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 251 |