Last synced on 14 November 2025 at 11:06 pm

DualX

Page Type
Cleared 510(K)
510(k) Number
K211740
510(k) Type
Special
Applicant
Amplify Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2021
Days to Decision
114 days
Submission Type
Summary

DualX

Page Type
Cleared 510(K)
510(k) Number
K211740
510(k) Type
Special
Applicant
Amplify Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2021
Days to Decision
114 days
Submission Type
Summary