Duns Number:824905723
Device Description: Femoral Stem, Lateral, Cementless, PC, Plasma
Catalog Number
1211-0-0050
Brand Name
TaperSet™ Hip System
Version/Model Number
1211-0-0050
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 28, 2021
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"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KWL
Product Code Name
Prosthesis, hip, hemi-, femoral, metal
Public Device Record Key
4751a699-5ad8-4df2-98d9-52538ae2099b
Public Version Date
July 29, 2021
Public Version Number
3
DI Record Publish Date
October 24, 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 | 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 |