Vertiflex (Tm), Incorporated
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Vertiflex (Tm), Incorporated makes
Vertiflex produces spinal fixation hardware, including the Vertiflex Spinal Screw System for surgical stabilization, and the Vertiflex Octane PEEK Vertebral Body Replacement (PEEK VBR) for interbody fusion in the lumbar spine.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is headquartered in the United States.
Catalogue
Vertiflex Spinal Screw System Ref K062670
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Vertiflex (Tm), Incorporated have in the registry?
The registry currently lists 2 devices for Vertiflex (Tm), Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertiflex (Tm), Incorporated's devices?
Among its 2 most recently registered devices, Vertiflex (Tm), Incorporated has devices listed in FDA 510(k) (2 devices).
What risk classes do Vertiflex (Tm), Incorporated's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vertiflex (Tm), Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertiflex (Tm), Incorporated in the registry?
The most recently registered devices listed for Vertiflex (Tm), Incorporated include VERTIFLEX SPINAL SCREW SYSTEM and VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR).