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

ELIBRA DYNAMIC KNEE BALANCER

K Number: K070108 · Decision Apr 4, 2007
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
16
Applicant Total
10
Review Days
83

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Basic Information

Device Name
ELIBRA DYNAMIC KNEE BALANCER
K Number
K070108
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synvasive Technology, Inc.
Date Received
January 11, 2007
Decision Date
April 4, 2007
Product Code
ONN
Advisory Committee
Neurology
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
ONN Intraoperative Orthopedic Joint Assessment Aid

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K950009 POWERGRIP(TM) COMPRESSION FIXATION DEVICE
K934336 SPINALPLANE
K933933 CEBOPLANE
K930573 SYNVASIVE CERAMIC SUTTING BLOCK
K932869 ARTHROPLANE
K931737 HEDLEYL INTRAMEDULLARY PREPARATION BRUSH