Signus Medizintechnik GmbH
FDA 510(k) & PMA Approved Devices — 21 products
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Total Devices21
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243188 | CYLOX® ST | OVE | 2025-02-11 | View |
| 510(k) | K241438 | Signus Tetris™ St; Signus Tetris™ R St | MAX | 2024-09-11 | View |
| 510(k) | K220658 | COSY Cervicothoracic Occipital Rod-Screw System | NKG | 2022-11-18 | View |
| 510(k) | K212755 | SIGNUS SACRONAIL® Transsacral Stabilization System | HWC | 2022-03-10 | View |
| 510(k) | K151704 | Diplomat® Spinal System | NKB | 2016-04-13 | View |
| 510(k) | K131372 | MOBIS II | MAX | 2013-07-02 | View |
| 510(k) | K122317 | TETRIS II | MAX | 2012-08-29 | View |
| 510(k) | K111792 | MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI | MAX | 2012-03-05 | View |
| 510(k) | K090387 | KAINOS+ | MQV | 2009-09-28 | View |
| 510(k) | K082848 | NUBIC AND RABEA DEVICES | ODP | 2009-07-24 | View |
| 510(k) | K081332 | ATHLET VERTEBRAL BODY REPLACEMENT SYSTEM | MQP | 2008-06-10 | View |
| 510(k) | K080815 | TOSCA II ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2008-04-23 | View |
| 510(k) | K080349 | KIMBA MINI | MQP | 2008-03-10 | View |
| 510(k) | K061082 | MOBIS SPINAL IMPLANT | MQP | 2006-12-18 | View |
| 510(k) | K061577 | OVALTWIST PEDICLE SCREW SYSTEM | MNH | 2006-09-14 | View |
| 510(k) | K052533 | KIMBA SPINAL IMPLANT | MQP | 2005-11-03 | View |
| 510(k) | K051659 | SEMIAL SPINAL IMPLANT | MQP | 2005-07-13 | View |
| 510(k) | K043316 | RABEA SPINAL IMPLANT | MQP | 2005-02-07 | View |
| 510(k) | K043082 | THE TOSCA ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2004-11-23 | View |
| 510(k) | K041888 | CURVED PEEK TETRIS SPINAL IMPLANT | MQP | 2004-08-10 | View |
No matching devices.
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