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GuideMia Ortho+

Page Type
Cleared 510(K)
510(k) Number
K162850
510(k) Type
Traditional
Applicant
GUIDEMIA TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
164 days
Submission Type
Statement

GuideMia Ortho+

Page Type
Cleared 510(K)
510(k) Number
K162850
510(k) Type
Traditional
Applicant
GUIDEMIA TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
164 days
Submission Type
Statement