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Orthosoft, Inc.

FDA 510(k) & PMA Approved Devices — 14 products

Total Devices14
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K131409 CAS PSI KNEE SYSTEMJWH2013-09-13 View
510(k) K100599 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 MMOLO2010-04-05 View
510(k) K071929 NAVITRACK SYSTEM- PARTIAL HIP RESURFACING UNIVERSALHAW2007-09-19 View
510(k) K071714 NAVITRACK SYSTEM - OS UNICONDYLAR KNEE UNIVERSAL, MODEL# PRO-06003HAW2007-07-20 View
510(k) K060336 NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002HAW2006-04-28 View
510(k) K043536 NAVITRACK SYSTEM - S&N IMAGE FREE KNEEHAW2005-01-14 View
510(k) K041369 NAVITRACK SYSTEM - S&N IMAGE FREE HIP, MODEL PRO-03017HAW2004-06-22 View
510(k) K032917 NAVITRACK SYSTEM - TOTAL HIP REPLACEMENT CT-FREEHAW2003-10-21 View
510(k) K030827 NAVITRACK SYSTEM: TOTAL HIP REPLACEMENT CT-FREE CUP, MODEL 900.204HAW2003-05-23 View
510(k) K031156 NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005HAW2003-05-09 View
510(k) K022364 NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200HAW2003-02-04 View
510(k) K021760 NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120HAW2002-08-27 View
510(k) K002053 NAVITRAK SYSTEM-OPTICAL OPTION, MODEL 900.004HAW2000-08-03 View
510(k) K981315 NAVITRACKHAW1998-07-09 View
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