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VERTIFLEX SPINOUS PROCESS FIXATION PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122509
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2012
Days to Decision
122 days
Submission Type
Summary

VERTIFLEX SPINOUS PROCESS FIXATION PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122509
510(k) Type
Traditional
Applicant
VERTIFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2012
Days to Decision
122 days
Submission Type
Summary