Last synced on 14 November 2025 at 11:06 pm

CYGNUS™ MoRe Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K220441
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2022
Days to Decision
212 days
Submission Type
Summary

CYGNUS™ MoRe Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K220441
510(k) Type
Traditional
Applicant
MiRus, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2022
Days to Decision
212 days
Submission Type
Summary