STELLAR Knee— 510(k) K232176
Substantially EquivalentPolarisar, Inc.
FDA 510(k) clearance K232176 for STELLAR Knee, Substantially Equivalent on 2023-11-02. Applicant: Polarisar, Inc.. Device class: 2.
Clearance details
- Applicant
- Polarisar, Inc.
- Product code
- Code SBF
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Recent devices under product code SBF
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