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ORTHOREX INTRA-OPERATIVE LOAD SENSOR

Page Type
Cleared 510(K)
510(k) Number
K090474
510(k) Type
Traditional
Applicant
ORTHOSENSOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2009
Days to Decision
237 days
Submission Type
Summary

ORTHOREX INTRA-OPERATIVE LOAD SENSOR

Page Type
Cleared 510(K)
510(k) Number
K090474
510(k) Type
Traditional
Applicant
ORTHOSENSOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2009
Days to Decision
237 days
Submission Type
Summary