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Intracept Intraosseous Nerve Ablation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222281
510(k) Type
Traditional
Applicant
Relievant Medsystems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2022
Days to Decision
89 days
Submission Type
Summary

Intracept Intraosseous Nerve Ablation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222281
510(k) Type
Traditional
Applicant
Relievant Medsystems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2022
Days to Decision
89 days
Submission Type
Summary