| Primary Device ID | 00613994207661 |
| NIH Device Record Key | 2102ca2c-a96a-47ea-9317-ebe893a54452 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TRAVERSE™ OCT Spinal Fixation System |
| Version Model Number | 7751012 |
| 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 |
| Length | 12 Millimeter |
| Length | 12 Millimeter |
| Length | 12 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 12 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994207661 [Primary] |
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
Moist Heat or Steam Sterilization
[00613994207661]
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 | 2015-07-07 |
| 00613994207661 | ROD 7751012 5.0X 12MM POSTED BONE SCREW |
| 00613994207654 | ROD 7751010EP 5.0X10MM EXT PST BONE SCRW |
| 00613994207647 | ROD 7751010 5.0X 10MM POSTED BONE SCREW |
| 00613994206374 | ROD 7751008EP 5.0X8MM EXT PST BONE SCRW |
| 00613994205643 | ROD 7750710EP 3.5X10MM EXT PST BONE SCRW |
| 00613994205612 | ROD 7751008 5.0X 8MM POSTED BONE SCREW |