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

UNICAP UNICOMPARTMENTAL KNEE RESURFACING PROSTHESIS

K Number: K050373 · Decision Oct 11, 2005
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
113
Applicant Total
26
Review Days
239

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Basic Information

Device Name
UNICAP UNICOMPARTMENTAL KNEE RESURFACING PROSTHESIS
K Number
K050373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrosurface, Inc.
Date Received
February 14, 2005
Decision Date
October 11, 2005
Product Code
HSX
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

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K173964 OVOMotion Shoulder Arthroplasty System
K172383 Arthrosurface Bone Screws
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K170350 ToeMATE® Hammertoe Correction System
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