EksoNR— 510(k) K220988
Substantially EquivalentEkso Bionics, Inc.
FDA 510(k) clearance K220988 for EksoNR, Substantially Equivalent on 2022-06-09. Applicant: Ekso Bionics, Inc.. Device class: 2.
Clearance details
- Applicant
- Ekso Bionics, Inc.
- Product code
- Code PHL
- Device class
- Class 2
- Regulation
- 21 CFR 890.3480
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Richmond, CA, US
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