Primary Device ID | 00846468087142 |
NIH Device Record Key | 1ecaed42-42ec-4f48-a1d3-cd8e2ac4a052 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fortilink®-L IBF System with TETRAfuse 3D Technology |
Version Model Number | 65-L-1440-8 |
Catalog Number | 65-L-1440-8 |
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 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00191083006819 [Primary] |
GS1 | 00846468087142 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
ODP | Intervertebral fusion device with bone graft, cervical |
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 |