Primary Device ID | 00763000085339 |
NIH Device Record Key | 8e3602f4-a77f-4912-98f5-34118c26ac47 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARTiC-L™ Spinal System |
Version Model Number | 5250900 |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000085339 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000085339]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-15 |
Device Publish Date | 2019-03-07 |
00763000085391 | TRIAL 5251500 L 25 HT 15 DEG 0 FIXED |
00763000085384 | TRIAL 5251400 L 25 HT 14 DEG 0 FIXED |
00763000085339 | TRIAL 5250900 L 25 HT 9 DEG 0 FIXED |
00763000085414 | TRIAL 5350800 L 35 HT 8 DEG 0 FIXED |
00763000085407 | TRIAL 5300800 L 30 HT 8 DEG 0 FIXED |
00763000085322 | TRIAL 5250800 L 25 HT 8 DEG 0 FIXED |
00763000085353 | TRIAL 5251100 L 25 HT 11 DEG 0 FIXED |
00763000085346 | TRIAL 5251000 L 25 HT 10 DEG 0 FIXED |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARTIC-L 87290814 5638538 Live/Registered |
Warsaw Orthopedic, Inc. 2017-01-05 |