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FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K091812
510(k) Type
Traditional
Applicant
FRONTIER DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2010
Days to Decision
323 days
Submission Type
Summary

FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K091812
510(k) Type
Traditional
Applicant
FRONTIER DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2010
Days to Decision
323 days
Submission Type
Summary