Spinalight, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K172536 | Atlas Percussion Adjusting Instrument | LXM | 2018-06-20 | View |
| 510(k) | K001476 | TORQUE INSTRUMENT, MODEL 8500 | LXM | 2000-08-04 | View |
| 510(k) | K955540 | HAND HELD ATLAS INSTRUMENT | LXM | 1996-03-04 | View |
| 510(k) | K946258 | MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENT | LXM | 1995-11-20 | View |
| 510(k) | K945954 | MODELS 4100 AND 4300 MULTITHERAPY | JFB | 1995-01-19 | View |
| 510(k) | K933622 | FLEXION DISTRACTION TABLE | INQ | 1994-01-07 | View |
| 510(k) | K933621 | HILO TABLE | INQ | 1994-01-07 | View |
No matching devices.
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