Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Plus Orthopedics

FDA 510(k) & PMA Approved Devices — 38 products

Total Devices38
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K032126 PROMOS SHOULDERHSD2004-01-08 View
510(k) K033763 MODIFICATION TO SLIM GLIDING NAIL SYSTEMKTT2003-12-18 View
510(k) K032709 MODULAR PLUS HIP STEMLWJ2003-09-23 View
510(k) K032548 IP-XS COMPRESSION NAIL SYSTEMHSB2003-09-10 View
510(k) K032215 VKS/TC-PLUS REVISION KNEEJWH2003-08-08 View
510(k) K032052 UC-PLUS SOLUTION UNICONDYLAR KNEEHRY2003-07-25 View
510(k) K031165 PLUS ORTHOPEDICS CEMENTED HIP STEMJDI2003-06-06 View
510(k) K030971 MODIFICATION TO MODULAR PLUS REVISION STEMLWJ2003-04-24 View
510(k) K024134 UNI HIP STEMLWJ2003-01-15 View
510(k) K023667 RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEEKRO2002-12-24 View
510(k) K023416 MODIFICATION TO VKS KNEE SYSTEMJWH2002-11-08 View
510(k) K022204 VKS KNEE SYSTEMJWH2002-10-18 View
510(k) K022120 MPF ACETABULAR CUP GENERATION 2LZO2002-07-24 View
510(k) K021714 RT-PLUS PE INSERT CLAMPKRO2002-06-21 View
510(k) K020298 GALILEO CAS/NAV TKR SYSTEMHAW2002-05-20 View
510(k) K021178 SL-PLUS LATERALIZED STEMJDI2002-05-14 View
510(k) K020240 SLIM GLIDING NAIL SYSTEMKTT2002-02-22 View
510(k) K013340 RT-PLUS KNEE ADDITIONAL COMPONENTSKRO2001-12-20 View
510(k) K011836 MPF ACETABULAR CUPLZO2001-09-07 View
510(k) K011719 PLUS CANCELLOUS BONE SCREWSHWC2001-07-02 View
↑