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

G4 SLEEVED NAIL

K Number: K020962 · Decision May 24, 2002
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
32
Review Days
60

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Basic Information

Device Name
G4 SLEEVED NAIL
K Number
K020962
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing, Inc.
Date Received
March 25, 2002
Decision Date
May 24, 2002
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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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
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