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VERTICALE® Posterior Spinal Fixation System/VERTICALE® System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171421
510(k) Type
Traditional
Applicant
Silony Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/10/2018
Days to Decision
240 days
Submission Type
Summary

VERTICALE® Posterior Spinal Fixation System/VERTICALE® System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171421
510(k) Type
Traditional
Applicant
Silony Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/10/2018
Days to Decision
240 days
Submission Type
Summary