| Primary Device ID | 00846468087173 |
| NIH Device Record Key | cd0f7943-472b-4018-93a5-3453fa470264 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fortilink®-L IBF System with TETRAfuse 3D Technology |
| Version Model Number | 65-L-1845-8 |
| Catalog Number | 65-L-1845-8 |
| Company DUNS | 793384496 |
| Company Name | Pioneer Surgical Technology, 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 | true |
| 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(386)418-8888 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00191083007267 [Primary] |
| GS1 | 00846468087173 [Primary] |
| MAX | Intervertebral fusion device with bone graft, lumbar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2018-08-24 |
| 00846468087234 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 22mm (W), 60mm (L |
| 00846468087227 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 22mm (W), 55mm (L |
| 00846468087210 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 22mm (W), 50mm (L |
| 00846468087203 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 22mm (W), 45mm (L |
| 00846468087197 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 18mm (W), 55mm (L |
| 00846468087180 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 18mm (W), 50mm (L |
| 00846468087173 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 18mm (W), 45mm (L |
| 00846468087166 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 14mm (W), 50mm (L |
| 00846468087159 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 14mm (W), 45mm (L |
| 00846468087142 | Fortilink-L Interbody Fusion Device (IBF) System with TETRAfuse 3D Technology, 14mm (W), 40mm (L |
| 00846468086756 | Fortilink-L IBF System Trial, 22mm (W) x 8mm (H) |
| 00846468086749 | Fortilink-L IBF System Trial, 18mm (W) x 8mm (H) |
| 00846468086732 | Fortilink-L IBF System Trial, 14mm (W) x 8mm (H) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FORTILINK 87101032 5287571 Live/Registered |
Pioneer Surgical Technology, Inc. 2016-07-12 |