Libertas E-XLPE Modular Liner— 510(k) K192989
Substantially EquivalentMaxx Orthopedics, Inc.
FDA 510(k) clearance K192989 for Libertas E-XLPE Modular Liner, Substantially Equivalent on 2020-10-29. Applicant: Maxx Orthopedics, Inc.. Device class: 2.
Clearance details
- Applicant
- Maxx Orthopedics, Inc.
- Product code
- Code OQI
- Device class
- Class 2
- Regulation
- 21 CFR 888.3353
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norristown, PA, US
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