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HyperFlex™ Bunion Correction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241995
510(k) Type
Traditional
Applicant
FootBridge Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2024
Days to Decision
140 days
Submission Type
Summary

HyperFlex™ Bunion Correction System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241995
510(k) Type
Traditional
Applicant
FootBridge Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2024
Days to Decision
140 days
Submission Type
Summary