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INTRACEPT Intraosseous Nerve Ablation System

Page Type
Cleared 510(K)
510(k) Number
K170827
510(k) Type
Traditional
Applicant
Relievant Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2017
Days to Decision
142 days
Submission Type
Summary

INTRACEPT Intraosseous Nerve Ablation System

Page Type
Cleared 510(K)
510(k) Number
K170827
510(k) Type
Traditional
Applicant
Relievant Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2017
Days to Decision
142 days
Submission Type
Summary