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Ancora LLC Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K143228
510(k) Type
Traditional
Applicant
FRONTIER MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2015
Days to Decision
108 days
Submission Type
Summary

Ancora LLC Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K143228
510(k) Type
Traditional
Applicant
FRONTIER MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2015
Days to Decision
108 days
Submission Type
Summary