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Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)

Page Type
Cleared 510(K)
510(k) Number
K180369
510(k) Type
Traditional
Applicant
Relievant Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2018
Days to Decision
214 days
Submission Type
Summary

Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)

Page Type
Cleared 510(K)
510(k) Number
K180369
510(k) Type
Traditional
Applicant
Relievant Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2018
Days to Decision
214 days
Submission Type
Summary