Wrist Hemiarthroplasty System— 510(k) K141920
Substantially EquivalentArthrosurface, Inc.
FDA 510(k) clearance K141920 for Wrist Hemiarthroplasty System, Substantially Equivalent on 2014-12-23. Applicant: Arthrosurface, Inc.. Device class: 2.
Clearance details
- Applicant
- Arthrosurface, Inc.
- Product code
- Code KWN
- Device class
- Class 2
- Regulation
- 21 CFR 888.3750
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Franklin, MA, US
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