Spinecraft, LLC
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System (K223301) | Spinecraft, LLC | 2023-07-20 |
| ASTRA Spine System (K223273) | Spinecraft, LLC | 2022-12-22 |
| ORIO-Ti Intervertebral Body Fusion Cage System (K211935) | Spinecraft, LLC | 2021-09-30 |
| ASTRA Spine System (K211323) | Spinecraft, LLC | 2021-06-03 |
| ASTRA-OCT Spine System (K181350) | Spinecraft, LLC | 2018-07-06 |
| APEX-DL Spine System (K143683) | Spinecraft, LLC | 2015-05-22 |
| ASTRA SPINE SYSTEM (K150417) | Spinecraft, LLC | 2015-05-19 |
| VELOX ANTERIOR CERVICAL PLATE SYSTEM (K131521) | Spinecraft, LLC | 2013-12-24 |
| APEX SPINE SYSTEM (K132603) | Spinecraft, LLC | 2013-11-20 |
| APEX SPINE SYSTEM (K110906) | Spinecraft, LLC | 2011-07-26 |
| ALTUM ANTERIOR CERVICAL PLATE (K103505) | Spinecraft, LLC | 2011-03-15 |
| APEX SPINE SYSTEM W/ COCR RODS (K102488) | Spinecraft, LLC | 2010-12-10 |
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