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Paramount Anterior Cervical Cage System

Page Type
Cleared 510(K)
510(k) Number
K173175
510(k) Type
Special
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2017
Days to Decision
33 days
Submission Type
Summary

Paramount Anterior Cervical Cage System

Page Type
Cleared 510(K)
510(k) Number
K173175
510(k) Type
Special
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2017
Days to Decision
33 days
Submission Type
Summary