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PlasmaBlade X 3.0S, PlasmaBlade X 4.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181257
510(k) Type
Traditional
Applicant
Medtronic Advanced Energy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2018
Days to Decision
83 days
Submission Type
Summary