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Longeviti ClearFit Cranial Implant

Page Type
Cleared 510(K)
510(k) Number
K203349
510(k) Type
Special
Applicant
Longeviti Neuro Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2020
Days to Decision
33 days
Submission Type
Summary

Longeviti ClearFit Cranial Implant

Page Type
Cleared 510(K)
510(k) Number
K203349
510(k) Type
Special
Applicant
Longeviti Neuro Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2020
Days to Decision
33 days
Submission Type
Summary