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Skyway Anterior Cervical Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250486
510(k) Type
Special
Applicant
Kyocera Medical Technologies, Inc. (KMTI)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
50 days
Submission Type
Summary

Skyway Anterior Cervical Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250486
510(k) Type
Special
Applicant
Kyocera Medical Technologies, Inc. (KMTI)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
50 days
Submission Type
Summary