FDA 510(k) Applications Submitted by VERTIFLEX (TM), INCORPORATED
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070218 | 01/23/2007 | VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR) | VERTIFLEX (TM), INCORPORATED |
| K062670 | 09/07/2006 | VERTIFLEX SPINAL SCREW SYSTEM | VERTIFLEX (TM), INCORPORATED |
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