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GR Splint Resin System

Page Type
Cleared 510(K)
510(k) Number
K211415
510(k) Type
Traditional
Applicant
Pro3dure Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/21/2021
Days to Decision
168 days
Submission Type
Summary

GR Splint Resin System

Page Type
Cleared 510(K)
510(k) Number
K211415
510(k) Type
Traditional
Applicant
Pro3dure Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/21/2021
Days to Decision
168 days
Submission Type
Summary