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C-MOR VISUALIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093717
510(k) Type
Traditional
Applicant
AXIS SURGICAL TECHNOLOGIES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2010
Days to Decision
90 days
Submission Type
Summary

C-MOR VISUALIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093717
510(k) Type
Traditional
Applicant
AXIS SURGICAL TECHNOLOGIES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2010
Days to Decision
90 days
Submission Type
Summary