Duns Number:830350380
Device Description: CEMENTSYS KPT1503-CDS AOIS XPDR 15/3
Catalog Number
-
Brand Name
KyphoPak™ Tray
Version/Model Number
KPT1503-CDS
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 29, 2018
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K041454
Product Code
HRX
Product Code Name
ARTHROSCOPE
Public Device Record Key
46a3dd13-7964-4f20-ba57-1017090b8d86
Public Version Date
July 06, 2018
Public Version Number
4
DI Record Publish Date
July 16, 2016
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 | 13352 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 26085 |
| 3 | A medical device with high risk that requires premarket approval | 190 |
| U | Unclassified | 75 |