# Vertiflex, Inc.

- Location (FDA's records): San Clamente, CA
- FDA decisions: 5 (2008–2012): 5 510(k) clearances
- Product codes: KWP (1), NKB (1), HRX (1), MNI (1), MAX (1)
- Predicates its devices cite: 20 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Sofamor Danek: 4 (https://510kreport.com/company/medtronic-sofamor-danek)
- Vertiflex (Tm), Incorporated: 3 (https://510kreport.com/company/vertiflex-tm)
- Lanx, Inc.: 2 (https://510kreport.com/company/lanx)
- Globus Medical, Inc.: 2 (https://510kreport.com/company/globus-medical)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)

## Firms that cite its devices most
- Exactech, Inc.: 3 (https://510kreport.com/company/exactech)
- Precision Spine, Inc.: 1 (https://510kreport.com/company/precision-spine)
- Reliance Medical Systems, LLC: 1 (https://510kreport.com/company/reliance-medical-systems)
- Choice Spine, LLC: 1 (https://510kreport.com/company/choice-spine)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)

## Its most-cited devices
- K122509: Vertiflex Spinous Process Fixation Plate (2012), cited by 3
- K082270: Octane Vertebral Body Replacement (VBR) System (2008), cited by 3
- K073245: Extended Vertiflex Spinal Screw System (2008), cited by 1

## Recent decisions
- K122509: Vertiflex Spinous Process Fixation Plate (Dec 17, 2012)
- K122662: Vertiflex Direct Decompression System (Nov 13, 2012)
- K082270: Octane Vertebral Body Replacement (VBR) System (Sep 16, 2008)
- K073143: Modified Vertiflex Spinal Screw System (Apr 7, 2008)
- K073245: Extended Vertiflex Spinal Screw System (Feb 15, 2008)

Source page: https://510kreport.com/company/vertiflex