Duns Number:046189866
Catalog Number
91-5709
Brand Name
TraumaOne SYSTEM
Version/Model Number
91-5709
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K143336,K152326,K202969
Product Code
DZL
Product Code Name
SCREW, FIXATION, INTRAOSSEOUS
Public Device Record Key
2b981d55-0106-46cb-b2d1-32608b01f529
Public Version Date
October 12, 2021
Public Version Number
2
DI Record Publish Date
June 18, 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 | 1783 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 11874 |
| 3 | A medical device with high risk that requires premarket approval | 34 |