FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

CAS FIXATION PIN 3.2 DIA X 180 MM STR, CAS FIXATON PIN 3.2 DIA X 80 MM STR, CAS FIXATON PIN 3.2 DIA X 150 MM

K Number: K100599 · Decision Apr 5, 2010
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
14
Review Days
33

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Basic Information

Device Name
CAS FIXATION PIN 3.2 DIA X 180 MM STR, CAS FIXATON PIN 3.2 DIA X 80 MM STR, CAS FIXATON PIN 3.2 DIA X 150 MM
K Number
K100599
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthosoft, Inc.
Date Received
March 3, 2010
Decision Date
April 5, 2010
Product Code
OLO
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
OLO Orthopedic Stereotaxic Instrument

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K030827 NAVITRACK SYSTEM: TOTAL HIP REPLACEMENT CT-FREE CUP, MODEL 900.204
K031156 NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005
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