FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MAESTRO TOTAL WRIST

K Number: K042032 · Decision Oct 7, 2004
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
16
Applicant Total
441
Review Days
71

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Basic Information

Device Name
MAESTRO TOTAL WRIST
K Number
K042032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3800
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet, Inc.
Date Received
July 28, 2004
Decision Date
October 7, 2004
Product Code
JWJ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JWJ Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained

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K212435 Comprehensive Humeral Fracture Positioning Sleeves
K210192 A.L.P.S. Clavicle Plating System
K193214 WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System, Biomet Headless Compression and Twist-Off Screws
K193546 Distal Centralizers
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