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VERTIFLEX SPINAL SCREW SYSTEM

Page Type
Cleared 510(K)
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)
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