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

TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE

K Number: K063515 · Decision Feb 2, 2007
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
90
Applicant Total
32
Review Days
73

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Basic Information

Device Name
TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE
K Number
K063515
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3530
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing, Inc.
Date Received
November 21, 2006
Decision Date
February 2, 2007
Product Code
HRY
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
HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

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Other Clearances by Biomet Manufacturing, Inc.

K Number Device Name
K130390 COMPREHENSIVE CONVERTIBLE GLENOID
K113271 METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
K113121 COMPREHENSIVE REVERSE SHOULDER
K080685 HIPLOC COMPRESSION HIP SCREW
K080088 BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
K071271 BIOMET CABLE SYSTEM
K070399 100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
K061340 23 MM SINGLE-PEG PATELLA COMPONENT
K061433 VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
K053505 REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS
Search all 32 clearances from Biomet Manufacturing, Inc. →