| Primary Device ID | 00763000031862 |
| NIH Device Record Key | b398bdac-be90-46f7-8ead-651d4c6e98ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BALLOON KYPHOPLASTY ESSENTIALS |
| Version Model Number | NH103PB |
| 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 | true |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000031862 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-26 |
| Device Publish Date | 2019-01-26 |
| 00763000031893 | KIT NH203PB 20/3 SPINE ESSEN FF |
| 00763000031886 | KIT NH153PB 15/3 SPINE ESSEN FF |
| 00763000031879 | KIT NH152PB 15/2 SPINE ESSEN FF |
| 00763000031862 | KIT NH103PB 10/3 SPINE ESSEN FF |
| 00763000031855 | KIT NH102PB 10/2 SPINE ESSEN FF |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BALLOON KYPHOPLASTY ESSENTIALS 86934265 5443850 Live/Registered |
Warsaw Orthopedic, Inc. 2016-03-09 |