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ORTHOVIS PREOPERATIVE PLAN

Page Type
Cleared 510(K)
510(k) Number
K133367
510(k) Type
Traditional
Applicant
CUSTOM ORTHOPAEDIC SOLUTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
49 days
Submission Type
Summary

ORTHOVIS PREOPERATIVE PLAN

Page Type
Cleared 510(K)
510(k) Number
K133367
510(k) Type
Traditional
Applicant
CUSTOM ORTHOPAEDIC SOLUTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
49 days
Submission Type
Summary