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Selectra Lead Implantation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222037
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2022
Days to Decision
8 days
Submission Type
Summary

Selectra Lead Implantation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222037
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2022
Days to Decision
8 days
Submission Type
Summary