Longeviti PorousFit implant— 510(k) K211514
Substantially EquivalentLongeviti Neuro Solutions, LLC
FDA 510(k) clearance K211514 for Longeviti PorousFit implant, Substantially Equivalent on 2021-07-15. Applicant: Longeviti Neuro Solutions, LLC. Device class: 2.
Clearance details
- Applicant
- Longeviti Neuro Solutions, LLC
- Product code
- Code KKY
- Device class
- Class 2
- Regulation
- 21 CFR 878.3500
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hunt Valley, MD, US
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