Last synced on 14 November 2025 at 11:06 pm

VERTIFLEX DIRECT DECOMPRESSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122662
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2012
Days to Decision
74 days
Submission Type
Summary

VERTIFLEX DIRECT DECOMPRESSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122662
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2012
Days to Decision
74 days
Submission Type
Summary