ClearPoint System— 510(k) K171257
Substantially EquivalentMri Interventions, Inc.
FDA 510(k) clearance K171257 for ClearPoint System, Substantially Equivalent on 2017-10-20. Applicant: Mri Interventions, Inc.. Device class: 2.
Clearance details
- Applicant
- Mri Interventions, Inc.
- Product code
- Code ORR
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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