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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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