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Ibis® Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K162995
510(k) Type
Traditional
Applicant
Ortho Development Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2017
Days to Decision
154 days
Submission Type
Summary

Ibis® Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K162995
510(k) Type
Traditional
Applicant
Ortho Development Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2017
Days to Decision
154 days
Submission Type
Summary