Duns Number:080506581
Device Description: TRI-LOCK BPS FEMORAL STEM 12/14 TAPER TRI-LOCK BPS W/GRIPTION SIZE 8 STD 111mm
Catalog Number
101204080
Brand Name
TRI-LOCK GRIPTION
Version/Model Number
1012-04-080
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P070026,K073570,P070026,P070026,P070026,P070026,P070026,P070026,P070026,P070026,P070026,P070026,P070026,P070026
Product Code
KWA
Product Code Name
Prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Public Device Record Key
e16b95c6-bccc-4823-8124-dbb2507bc11e
Public Version Date
May 11, 2022
Public Version Number
4
DI Record Publish Date
March 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 | 5254 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4003 |
| 3 | A medical device with high risk that requires premarket approval | 908 |