Last synced on 30 September 2022 at 11:05 pm

GuideMia Ortho+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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