Primary Device ID | 00819251029643 |
NIH Device Record Key | 8313d336-37d1-45d4-82ad-b5c9c5db116b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Femoral Cut Block, Central Capture, Klassic ONE |
Version Model Number | 2141.05.000 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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 |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
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 | 00819251029643 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
[00819251029643]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-20 |
Device Publish Date | 2021-09-10 |
00819251029667 | Femoral Cut Block, Central Capture, Size 7 |
00819251029650 | Femoral Cut Block, Central Capture, Size 6 |
00819251029643 | Femoral Cut Block, Central Capture, Size 5 |
00819251029636 | Femoral Cut Block, Central Capture, Size 4 |
00819251029629 | Femoral Cut Block, Central Capture, Size 3 |
00819251029612 | Femoral Cut Block, Central Capture, Size 2 |
00819251029605 | Femoral Cut Block, Central Capture, Size 1 |