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MODIFIED VERTIFLEX SPINAL SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073143
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2008
Days to Decision
152 days
Submission Type
Summary

MODIFIED VERTIFLEX SPINAL SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073143
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2008
Days to Decision
152 days
Submission Type
Summary