Last synced on 14 November 2025 at 11:06 pm

MAKO Device

Page Type
Cleared 510(K)
510(k) Number
K151275
510(k) Type
Traditional
Applicant
nVision Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2015
Days to Decision
184 days
Submission Type
Summary

MAKO Device

Page Type
Cleared 510(K)
510(k) Number
K151275
510(k) Type
Traditional
Applicant
nVision Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2015
Days to Decision
184 days
Submission Type
Summary