Plus Orthopedics
Plus Orthopedics holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2004.
Top product codes for Plus Orthopedics
Recent clearances by Plus Orthopedics
- K032126 — PROMOS SHOULDER
- K033763 — MODIFICATION TO SLIM GLIDING NAIL SYSTEM
- K032709 — MODULAR PLUS HIP STEM
- K032548 — IP-XS COMPRESSION NAIL SYSTEM
- K032215 — VKS/TC-PLUS REVISION KNEE
- K032052 — UC-PLUS SOLUTION UNICONDYLAR KNEE
- K031165 — PLUS ORTHOPEDICS CEMENTED HIP STEM
- K030971 — MODIFICATION TO MODULAR PLUS REVISION STEM
- K024134 — UNI HIP STEM
- K023667 — RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
- K023416 — MODIFICATION TO VKS KNEE SYSTEM
- K022204 — VKS KNEE SYSTEM
- K022120 — MPF ACETABULAR CUP GENERATION 2
- K021714 — RT-PLUS PE INSERT CLAMP
- K020298 — GALILEO CAS/NAV TKR SYSTEM
- K021178 — SL-PLUS LATERALIZED STEM
- K020240 — SLIM GLIDING NAIL SYSTEM
- K013340 — RT-PLUS KNEE ADDITIONAL COMPONENTS
- K011836 — MPF ACETABULAR CUP
- K011719 — PLUS CANCELLOUS BONE SCREWS
- K011258 — TC-PLUS POROUS FEMORAL COMPONENTS
- K011288 — TC-PLUS POROUS TIBIAL COMPONENTS
- K003504 — RT-PLUS MODULAR CEMENTED KNEE COMPONENTS
- K003274 — LPC-PLUS ACETABULAR CUP
- K994146 — EPF-PLUS CEMENTLESS PRESS-FIT ACETABULAR CUP
- K000666 — TC-PLUS SOLUTION KNEE
- K001942 — SL-PLUS AND SLR-PLUS STEMS
- K993874 — BOFOR REVISION COUP
- K994126 — MODULAR-PLUS REVISION STEM
- K992154 — BICON-PLUS ACETABULAR COMPONENTS
- K992153 — PE-PLUS ACETABULAR CUP
- K990261 — PLUS CERAMIC HEAD PROSTHESES (ALUMINA AND ZIRKONIA)
- K982859 — UC-PLUS SOLUTION UNICONDYLAR KNEE SYSTEM
- K990309 — PLUS FRACTURE HEAD PROSTHESIS
- K982447 — PLUS BIPOLAR PROSTHESIS COCRMO
- K974409 — FRIEDL GLIDING NAIL SYSTEM
- K973077 — PLUS-FIT ACETABULAR CUP
- K973098 — COMPRESSION CERCLAGE GUNDOLF CCG-GF
Data sourced from openFDA. This site is unofficial and independent of the FDA.