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Patient Specific Marking Guides

Page Type
Cleared 510(K)
510(k) Number
K211076
510(k) Type
Traditional
Applicant
Additive Orthopaedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2022
Days to Decision
442 days
Submission Type
Summary

Patient Specific Marking Guides

Page Type
Cleared 510(K)
510(k) Number
K211076
510(k) Type
Traditional
Applicant
Additive Orthopaedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2022
Days to Decision
442 days
Submission Type
Summary