| Primary Device ID | 00613994490346 |
| NIH Device Record Key | 0409510d-33d7-4c24-9959-07d03089ea48 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PRESTIGE LP™ |
| Version Model Number | 6972525 |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Height | 5 Millimeter |
| Height | 5 Millimeter |
| Height | 5 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Depth | 12 Millimeter |
| Height | 5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994490346 [Primary] |
| MJO | PROSTHESIS, INTERVERTEBRAL DISC |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
Moist Heat or Steam Sterilization
[00613994490346]
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 | 2016-08-28 |
| 00613994714831 | INNER SHAFT 6973050 5MM INSERTER US |
| 00613994493743 | DISC 6972250 PRESTIGE |
| 00613994493712 | DISC 6972450 PRESTIGE |
| 00613994493675 | DISC 6972650 PRESTIGE |
| 00613994490735 | PUNCH 6972425 RAIL |
| 00613994490711 | PUNCH 6972445 RAIL |
| 00613994490476 | TRIAL 6973225 IMPLANT |
| 00613994490452 | TRIAL 6973245 IMPLANT |
| 00613994490414 | TRIAL 6973265 IMPLANT |
| 00613994490346 | GUIDE 6972525 CUTTER |
| 00613994490322 | GUIDE 6972545 CUTTER |