Orthosoft, Inc.
Orthosoft, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2013.
Top product codes for Orthosoft, Inc.
Recent clearances by Orthosoft, Inc.
- K131409 — CAS PSI KNEE SYSTEM
- 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 MM
- 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
- K022364 — NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200
- K021760 — NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120
- K002053 — NAVITRAK SYSTEM-OPTICAL OPTION, MODEL 900.004
- K981315 — NAVITRACK
Data sourced from openFDA. This site is unofficial and independent of the FDA.