Duns Number:824905723
Device Description: Knee System
Catalog Number
4000-0-1000
Brand Name
TracPatch
Version/Model Number
4000-0-1000
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KQX
Product Code Name
Goniometer, ac-powered
Public Device Record Key
5aec659d-1127-4b00-817e-43c80f69603d
Public Version Date
April 03, 2020
Public Version Number
1
DI Record Publish Date
March 26, 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 | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2053 |
| 3 | A medical device with high risk that requires premarket approval | 85 |