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OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250213
510(k) Type
Traditional
Applicant
Stryker Instruments
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2025
Days to Decision
111 days
Submission Type
Summary

OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250213
510(k) Type
Traditional
Applicant
Stryker Instruments
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2025
Days to Decision
111 days
Submission Type
Summary