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VERTIFLEX SPINAL SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062670
510(k) Type
Traditional
Applicant
Vertiflex (Tm), Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2007
Days to Decision
127 days
Submission Type
Summary

VERTIFLEX SPINAL SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062670
510(k) Type
Traditional
Applicant
Vertiflex (Tm), Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2007
Days to Decision
127 days
Submission Type
Summary