Primary Device ID | 00643169524040 |
NIH Device Record Key | 68bd34c7-b60c-4f46-a052-7f54ffd4ee43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System |
Version Model Number | 2156616 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, 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(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.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 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00643169524040 [Primary] |
KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
[00643169524040]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-04-09 |
00643169524880 | GUIDE 2160220 ALIF SCREW GUIDE 20MM |
00643169524873 | GUIDE 2160218 ALIF SCREW GUIDE 18MM |
00643169524866 | GUIDE 2160216 ALIF SCREW GUIDE 16MM |
00643169524859 | GUIDE 2160214 ALIF SCREW GUIDE 14MM |
00643169524842 | GUIDE 2160212 ALIF SCREW GUIDE 12MM |
00643169524835 | GUIDE 2160210 ALIF SCREW GUIDE 10MM |
00643169524828 | GUIDE 2150220 O51 SCREW GUIDE 20MM |
00643169524811 | GUIDE 2150218 O51 SCREW GUIDE 18MM |
00643169524804 | GUIDE 2150216 O51 SCREW GUIDE 16MM |
00643169524798 | GUIDE 2150214 O51 SCREW GUIDE 14MM |
00643169524781 | GUIDE 2150212 O51 SCREW GUIDE 12MM |
00643169524774 | GUIDE 2150210 O51 SCREW GUIDE 10MM |
00643169524767 | INSERTER 2160400 ALIF FREEHAND |
00643169524750 | INSERTER 2160300 ALIF SIMPLE PLATE |
00643169524743 | INSERTER 2160200 ALIF SIMPLE INTERBODY |
00643169524712 | REMOVER 2151150 INTERBODY REMOVER |
00643169524682 | INSERTER 2151100 HANDLE INSERTER |
00643169524644 | INSERTER 2150200 O51 SIMPLE INTERBODY |
00643169524637 | INSERTER 2150300 O51 SIMPLE PLATE |
00643169524620 | HANDLE 2150330 TRIAL HANDLE |
00643169524613 | HANDLE 2150340 PLATE TRIAL HANDLE |
00643169524606 | INSERTER 2150400 O51 FREEHAND |
00643169524545 | TRAY 2159004 DIVERGENCE-L TRIALS |
00643169524491 | TRIAL 2156420 SMALL 6 DEGREES 20MM |
00643169524484 | TRIAL 2156418 SMALL 6 DEGREES 18MM |
00643169524477 | TRIAL 2156416 SMALL 6 DEGREES 16MM |
00643169524460 | TRIAL 2156414 SMALL 6 DEGREES 14MM |
00643169524453 | TRIAL 2156412 SMALL 6 DEGREES 12MM |
00643169524446 | TRIAL 2156410 SMALL 6 DEGREES 10MM |
00643169524439 | TRIAL 2154620 LARGE 24 DEGREES 20MM |
00643169524422 | TRIAL 2154618 LARGE 24 DEGREES 18MM |
00643169524415 | TRIAL 2154520 MEDIUM 24 DEGREES 20MM |
00643169524408 | TRIAL 2154518 MEDIUM 24 DEGREES 18MM |
00643169524392 | TRIAL 2154516 MEDIUM 24 DEGREES 16MM |
00643169524385 | TRIAL 2154420 SMALL 24 DEGREES 20MM |
00643169524378 | TRIAL 2154418 SMALL 24 DEGREES 18MM |
00643169524361 | TRIAL 2154416 SMALL 24 DEGREES 16MM |
00643169524354 | TRIAL 2152620 LARGE 12 DEGREES 20MM |
00643169524347 | TRIAL 2152618 LARGE 12 DEGREES 18MM |
00643169524330 | TRIAL 2152616 LARGE 12 DEGREES 16MM |
00643169524323 | TRIAL 2152614 LARGE 12 DEGREES 14MM |
00643169524316 | TRIAL 2152612 LARGE 12 DEGREES 12MM |
00643169524309 | TRIAL 2152520 MEDIUM 12 DEGREES 20MM |
00643169524293 | TRIAL 2152518 MEDIUM 12 DEGREES 18MM |
00643169524286 | TRIAL 2152516 MEDIUM 12 DEGREES 16MM |
00643169524279 | TRIAL 2152514 MEDIUM 12 DEGREES 14MM |
00643169524262 | TRIAL 2152512 MEDIUM 12 DEGREES 12MM |
00643169524255 | TRIAL 2152510 MEDIUM 12 DEGREES 10MM |
00643169524248 | TRIAL 2152420 SMALL 12 DEGREES 20MM |
00643169524231 | TRIAL 2150316 PLATE TRIAL 16MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIVERGENCE-L 86438209 4871814 Live/Registered |
Warsaw Orthopedic, Inc. 2014-10-29 |