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Aurora Surgiscope System

Page Type
Cleared 510(K)
510(k) Number
K182211
510(k) Type
Traditional
Applicant
Rebound Therapeutics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2019
Days to Decision
156 days
Submission Type
Summary

Aurora Surgiscope System

Page Type
Cleared 510(K)
510(k) Number
K182211
510(k) Type
Traditional
Applicant
Rebound Therapeutics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2019
Days to Decision
156 days
Submission Type
Summary