Spine Wave, Inc.
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopol recall (Z-1960-2015) | Spine Wave, Inc. | 2015-07-02 |
| StaXx IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar; recall (Z-2187-2013) | Spine Wave, Inc. | 2013-09-11 |
| StaXx XD Expandable Cartridge Convex Expandable Implant 25mm (L) x 9mm (W) x 7mm (H) Catal recall (Z-0967-2011) | Spine Wave Inc | 2011-01-26 |
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Every clearance here is in the API, with alerts when new ones post.