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Ancora LLC Interbody Fusion Device

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