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Spine Wave Gen II Expandable Interbody System

Page Type
Cleared 510(K)
510(k) Number
K152620
510(k) Type
Traditional
Applicant
SPINE WAVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2016
Days to Decision
123 days
Submission Type
Summary

Spine Wave Gen II Expandable Interbody System

Page Type
Cleared 510(K)
510(k) Number
K152620
510(k) Type
Traditional
Applicant
SPINE WAVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2016
Days to Decision
123 days
Submission Type
Summary