Medical Device Manufacturer · US , Carlsbad , CA

Vertiflex (Tm), Incorporated - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vertiflex (Tm), Incorporated Orthopedic ✕
2 devices
1-2 of 2
Cleared Apr 06, 2007
VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR)
K070218 · MQP
Orthopedic · 73d
Cleared Jan 12, 2007
VERTIFLEX SPINAL SCREW SYSTEM
K062670 · MNH
Orthopedic · 127d
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