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ProxiFuse Hammer Toe Device

Page Type
Cleared 510(K)
510(k) Number
K142490
510(k) Type
Traditional
Applicant
Cartiva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2014
Days to Decision
102 days
Submission Type
Summary

ProxiFuse Hammer Toe Device

Page Type
Cleared 510(K)
510(k) Number
K142490
510(k) Type
Traditional
Applicant
Cartiva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2014
Days to Decision
102 days
Submission Type
Summary