Monteris Medical NeuroBlate System— 510(k) K240877
Substantially EquivalentMonteris Medical,
FDA 510(k) clearance K240877 for Monteris Medical NeuroBlate System, Substantially Equivalent on 2024-06-04. Applicant: Monteris Medical,. Device class: 2.
Clearance details
- Applicant
- Monteris Medical,
- Product code
- Code ONO
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minnetonka, MN, US
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