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Impulse AM Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K210090
510(k) Type
Traditional
Applicant
DeGen Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2021
Days to Decision
229 days
Submission Type
Summary

Impulse AM Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K210090
510(k) Type
Traditional
Applicant
DeGen Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2021
Days to Decision
229 days
Submission Type
Summary