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Longeviti ClearFit Cranial Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202901
510(k) Type
Special
Applicant
Longeviti Neuro Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2020
Days to Decision
31 days
Submission Type
Statement

Longeviti ClearFit Cranial Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202901
510(k) Type
Special
Applicant
Longeviti Neuro Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2020
Days to Decision
31 days
Submission Type
Statement