| Primary Device ID | 00846468092917 |
| NIH Device Record Key | b610140a-1391-48aa-98a0-ce529535dbc0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fortilink-A IBF System |
| Version Model Number | 65-A-M16-8L |
| Catalog Number | 65-A-M16-8L |
| Company DUNS | 793384496 |
| Company Name | Pioneer Surgical Technology, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
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| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Phone | +1(906)226-9909 |
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| Device Size Text, specify | 0 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846468092917 [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 | 2020-01-10 |
| 00846468098414 | V Shape Tamp |
| 00846468094010 | Interbody Fusion Device |
| 00846468094003 | Interbody Fusion Device |
| 00846468093990 | Interbody Fusion Device |
| 00846468093983 | Interbody Fusion Device |
| 00846468093976 | Interbody Fusion Device |
| 00846468093969 | Interbody Fusion Device |
| 00846468093952 | Interbody Fusion Device |
| 00846468093945 | Interbody Fusion Device |
| 00846468093938 | Interbody Fusion Device |
| 00846468093921 | Interbody Fusion Device |
| 00846468093914 | Interbody Fusion Device |
| 00846468093907 | Interbody Fusion Device |
| 00846468093891 | Anterior Trial Spacer |
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