Spinous process plate
FDA product code PEK · Class 2 · 10 devices · 10 reports · 0 devices named in recalls
- SP-FIX 188.044Globus Medical, Inc. · Spinous process plate1 report
- SP-FIX 588.026Globus Medical, Inc. · Spinous process plate1 report
- CoFix Implant 10 mm RQI00010Paradigm Spine GmbH · Spinous Process Plate1 report
- UniVise 48590035Stryker Corporation · Spinous process plate1 report
- ROMEO 2 PAD POSTERIOR AXIAL DEVICE PAD-IM TI 08-SSpineArt SA · Spinous Process Plate1 report
- ZIP ULTRAAurora Spine, Inc. · Spinous Process Plate1 report
- ZIP LPAurora Spine, Inc. · Spinous Process Plate1 report
- ZIP LPAurora Spine, Inc. · Spinous Process Plate1 report
- Axle Interspinous Fusion System X060-0080Xtant Medical Holdings, Inc. · Spinous process plate1 report
- Axle Interspinous Fusion System X060-0241Xtant Medical Holdings, Inc. · Spinous process plate1 report