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FDA 510(k), K200718, Arthrosurface WristMotion Total Wrist Arthroplasty System
FDA 510(k), K200718, Arthrosurface WristMotion Total Wrist Arthroplasty System
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$170.23 USD
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510(K) Number: K200718
Device Name: Arthrosurface WristMotion Total Wrist Arthroplasty System
Manufacturer: Arthrosurface, Inc.
Device Classification Name: Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
Regulation Number: 888.3800
Classification Product Code: JWJ
Date Received: 03/19/2020
Decision Date: 10/15/2020
Regulation Medical Specialty: Orthopedic
Total Pages: 378
Fully Redacted Pages: 324
Content Pages: 54
Device Name: Arthrosurface WristMotion Total Wrist Arthroplasty System
Manufacturer: Arthrosurface, Inc.
Device Classification Name: Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
Regulation Number: 888.3800
Classification Product Code: JWJ
Date Received: 03/19/2020
Decision Date: 10/15/2020
Regulation Medical Specialty: Orthopedic
Total Pages: 378
Fully Redacted Pages: 324
Content Pages: 54
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