SmartFlow Neuro Cannula— 510(k) DEN240023
UnknownClearPoint Neuro, Inc.
FDA 510(k) clearance DEN240023 for SmartFlow Neuro Cannula, Unknown on 2024-11-13. Applicant: ClearPoint Neuro, Inc.. Device class: 2.
Clearance details
- Applicant
- ClearPoint Neuro, Inc.
- Product code
- Code SDG
- Device class
- Class 2
- Regulation
- 21 CFR 882.4110
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Solana Beach, CA, US
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