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OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device

Page Type
Cleared 510(K)
510(k) Number
K221074
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2022
Days to Decision
157 days
Submission Type
Summary

OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device

Page Type
Cleared 510(K)
510(k) Number
K221074
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2022
Days to Decision
157 days
Submission Type
Summary