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VUSION(R) OS

Page Type
Cleared 510(K)
510(k) Number
K111965
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2011
Days to Decision
106 days
Submission Type
Summary

VUSION(R) OS

Page Type
Cleared 510(K)
510(k) Number
K111965
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2011
Days to Decision
106 days
Submission Type
Summary