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

NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120

K Number: K021760 · Decision Aug 27, 2002
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
14
Review Days
90

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Basic Information

Device Name
NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120
K Number
K021760
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
May 29, 2002
Decision Date
August 27, 2002
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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Other Clearances by Orthosoft, Inc.

K Number Device Name
K131409 CAS PSI KNEE SYSTEM
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K071929 NAVITRACK SYSTEM- PARTIAL HIP RESURFACING UNIVERSAL
K071714 NAVITRACK SYSTEM - OS UNICONDYLAR KNEE UNIVERSAL, MODEL# PRO-06003
K060336 NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002
K043536 NAVITRACK SYSTEM - S&N IMAGE FREE KNEE
K041369 NAVITRACK SYSTEM - S&N IMAGE FREE HIP, MODEL PRO-03017
K032917 NAVITRACK SYSTEM - TOTAL HIP REPLACEMENT CT-FREE
K030827 NAVITRACK SYSTEM: TOTAL HIP REPLACEMENT CT-FREE CUP, MODEL 900.204
K031156 NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005
Search all 14 clearances from Orthosoft, Inc. →