Primary Device ID | 00814703015670 |
NIH Device Record Key | cef2a3ef-880a-4e80-870b-fd9a278c67aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Klassic Femur, PS-Post |
Version Model Number | 5101.03.000 |
Company DUNS | 078416717 |
Company Name | TOTAL JOINT ORTHOPEDICS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(801)486-6070 |
udi@tjoinc.com |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814703015670 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00814703015670]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-24 |
Device Publish Date | 2019-04-16 |
00814703015717 | Femur, PS-Post, Size 7 |
00814703015700 | Femur, PS-Post, Size 6 |
00814703015694 | Femur, PS-Post, Size 5 |
00814703015687 | Femur, PS-Post, Size 4 |
00814703015670 | Femur, PS-Post, Size 3 |
00814703015663 | Femur, PS-Post, Size 2 |
00814703015656 | Femur, PS-Post, Size 1 |