Last synced on 14 November 2025 at 11:06 pm

Phoenix Sinus Tarsi Stent System

Page Type
Cleared 510(K)
510(k) Number
K251382
510(k) Type
Traditional
Applicant
Astra Orthomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2025
Days to Decision
117 days
Submission Type
Summary

Phoenix Sinus Tarsi Stent System

Page Type
Cleared 510(K)
510(k) Number
K251382
510(k) Type
Traditional
Applicant
Astra Orthomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2025
Days to Decision
117 days
Submission Type
Summary