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DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional

Page Type
Cleared 510(K)
510(k) Number
K192702
510(k) Type
Traditional
Applicant
Synthes (USA) Products LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2020
Days to Decision
357 days
Submission Type
Summary

DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional

Page Type
Cleared 510(K)
510(k) Number
K192702
510(k) Type
Traditional
Applicant
Synthes (USA) Products LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2020
Days to Decision
357 days
Submission Type
Summary