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DePuy Synthes Craniomaxillofacial Sternal Devices - MR Conditional

Page Type
Cleared 510(K)
510(k) Number
K190963
510(k) Type
Traditional
Applicant
Synthes (Usa) Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2019
Days to Decision
102 days
Submission Type
Summary

DePuy Synthes Craniomaxillofacial Sternal Devices - MR Conditional

Page Type
Cleared 510(K)
510(k) Number
K190963
510(k) Type
Traditional
Applicant
Synthes (Usa) Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2019
Days to Decision
102 days
Submission Type
Summary