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Flex Robotic System and Flex Colorectal Drive

Page Type
Cleared 510(K)
510(k) Number
K162330
510(k) Type
Traditional
Applicant
Medrobotics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2017
Days to Decision
258 days
Submission Type
Summary

Flex Robotic System and Flex Colorectal Drive

Page Type
Cleared 510(K)
510(k) Number
K162330
510(k) Type
Traditional
Applicant
Medrobotics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2017
Days to Decision
258 days
Submission Type
Summary