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BostonSight PD Prosthetic Device

Page Type
Cleared 510(K)
510(k) Number
K161461
510(k) Type
Traditional
Applicant
BostonSight
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2016
Days to Decision
60 days
Submission Type
Summary

BostonSight PD Prosthetic Device

Page Type
Cleared 510(K)
510(k) Number
K161461
510(k) Type
Traditional
Applicant
BostonSight
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2016
Days to Decision
60 days
Submission Type
Summary