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

BIOMET FEMORAL LOCKING NAIL SYSTEM

K Number: K072161 · Decision Sep 20, 2007
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
93
Review Days
45

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Basic Information

Device Name
BIOMET FEMORAL LOCKING NAIL SYSTEM
K Number
K072161
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 Corp
Date Received
August 6, 2007
Decision Date
September 20, 2007
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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