FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS

K Number: K113271 · Decision May 18, 2012
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
32
Review Days
196

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Basic Information

Device Name
METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
K Number
K113271
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing, Inc.
Date Received
November 4, 2011
Decision Date
May 18, 2012
Product Code
KWA
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
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

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K071271 BIOMET CABLE SYSTEM
K070399 100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
K063515 TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE
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
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