Medical Device Manufacturer · CA , Montreal, Quebec

Orthosoft, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1998

Total

Cleared

Denied

Orthosoft, Inc. has 14 FDA 510(k) cleared neurology devices. Based in Montreal, Quebec, CA.

Historical record: 14 cleared submissions from 1998 to 2013.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Orthosoft, Inc.

14 devices

1-14 of 14

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

K100599 · OLO

Orthopedic · 33d

Cleared Sep 19, 2007

NAVITRACK SYSTEM- PARTIAL HIP RESURFACING UNIVERSAL

K071929 · HAW

Neurology · 68d

Cleared Jul 20, 2007

NAVITRACK SYSTEM - OS UNICONDYLAR KNEE UNIVERSAL, MODEL# PRO-06003

K071714 · HAW

Neurology · 28d

Cleared Apr 28, 2006

NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002

K060336 · HAW

Neurology · 77d

Cleared Jan 14, 2005

NAVITRACK SYSTEM - S&N IMAGE FREE KNEE

K043536 · HAW

Neurology · 23d

Cleared Jun 22, 2004

NAVITRACK SYSTEM - S&N IMAGE FREE HIP, MODEL PRO-03017

K041369 · HAW

Neurology · 29d

Cleared Oct 21, 2003

NAVITRACK SYSTEM - TOTAL HIP REPLACEMENT CT-FREE

K032917 · HAW

Neurology · 29d

Cleared May 23, 2003

NAVITRACK SYSTEM: TOTAL HIP REPLACEMENT CT-FREE CUP, MODEL 900.204

K030827 · HAW

Neurology · 70d

Cleared May 09, 2003

NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005

K031156 · HAW

Neurology · 28d

Cleared Feb 04, 2003

NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200

K022364 · HAW

Neurology · 197d

Cleared Aug 27, 2002

NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120

K021760 · HAW

Neurology · 90d

Cleared Aug 03, 2000

NAVITRAK SYSTEM-OPTICAL OPTION, MODEL 900.004

Orthosoft, Inc. - FDA 510(k) Cleared Devices

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