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ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121702
510(k) Type
Traditional
Applicant
Orthocor Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2013
Days to Decision
332 days
Submission Type
Summary

ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121702
510(k) Type
Traditional
Applicant
Orthocor Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2013
Days to Decision
332 days
Submission Type
Summary