Primary Device ID | 00673978130965 |
NIH Device Record Key | faa7d582-9a3f-4b96-8f0c-6dd90aa7070c |
Commercial Distribution Discontinuation | 2018-10-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | DYNA-LOK® Spinal System |
Version Model Number | X0197-032 |
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 | true |
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 |
Width | 14 Millimeter |
Width | 14 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00673978130965 [Primary] |
MNH | Orthosis, spondylolisthesis spinal fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00673978130965]
Moist Heat or Steam Sterilization
[00673978130965]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-06 |
Device Publish Date | 2015-08-18 |
00673978150864 | DYN 10-32 NUT TI |
00673978150857 | DYN 10MM 10-32 STUD TI |
00673978130972 | DYN 16MM 10-32 STUD TI |
00673978130965 | DYN 14MM 10-32 STUD TI |
00673978130958 | DYN 12MM 10-32 STUD TI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DYNA-LOK 74180852 1767986 Dead/Cancelled |
WARSAW ORTHOPEDIC, INC. 1991-07-01 |
DYNA-LOK 73335326 1247560 Dead/Cancelled |
ITT Grinnell Valve Co., Inc. 1981-11-02 |