7853a86800406a22e090fbd4fbc291d0

INSTRUMENTAL DE PLACA PARA FRACTURA PERI-PROTÉSICA DE ÁNGULO VARIABLE

PLATE INSTRUMENTS FOR PERI-PROSTHETIC FRACTURE OF VARIABLE ANGLE
JOHNSON & JOHNSON MEDTECH COLOMBIA S.A.S.·IIa·Colombia INVIMA·Expires April 09, 2034
Device classification
Risk class / Clase de Riesgo
IIa
Product type (Spanish)
MEDICO QUIRURGICOS
Product type (English)
SURGICAL DOCTOR
Registration information
Analysis ID
7853a86800406a22e090fbd4fbc291d0
Expire date
April 09, 2034
Authorized company / Fabricante
Name (English)
JOHNSON & JOHNSON MEDTECH COLOMBIA S.A.S.
Product use / Uso del Producto
Spanish

EL SISTEMA DE PLACAS PARA FÉMUR PROXIMAL PERIPROTÉSICO DE ÁNGULO VARIABLE LCP™ DE 3.5/4.5 MM CONSISTE EN SOLUCIONES DE PLACAS PARA FRACTURAS PERIPROTÉSICAS ALREDEDOR DE UNA PRÓTESIS DE CADERA. ESTÁN INDICADAS PARA EL TRATAMIENTO DE FRACTURAS PERIPROTÉSICAS Y FRACTURAS EN PRESENCIA DE IMPLANTES INTRAMEDULARES EN EL SEGMENTO DEL EXTREMO PROXIMAL Y EL 1/3 PROXIMAL Y MEDIO DEL SEGMENTO DIAFISARIO DEL FÉMUR, Y NO UNIONES O MAL UNIONES DE TALES FRACTURAS, EN PACIENTES ADULTOS, PARTICULARMENTE EN HUESO OSTEOPORÓTICO Y OSTEOPÉNICO _x000D_ _x000D_ _x000D_

English

THE 3.5/4.5 MM LCP™ VARIABLE ANGLE PERIPROSTHETIC PROXIMAL FEMUR PLATE SYSTEM CONSISTS OF PLATE SOLUTIONS FOR PERIPROSTHETIC FRACTURES AROUND A HIP REPLACEMENT. THEY ARE INDICATED FOR THE TREATMENT OF PERIPROSTHETIC FRACTURES AND FRACTURES IN THE PRESENCE OF INTRAMEDULLARY IMPLANTS IN THE PROXIMAL END SEGMENT AND THE PROXIMAL AND MIDDLE 1/3 OF THE DIAPHYSEAL SEGMENT OF THE FEMUR, AND NOT UNIONS OR MALUNIONS OF SUCH FRACTURES, IN ADULT PATIENTS, PARTICULARLY IN OSTEOPOROTIC AND OSTEOPENIC BONE _x000D_ _x000D_ _x000D_

About this record

Access comprehensive regulatory information for INSTRUMENTAL DE PLACA PARA FRACTURA PERI-PROTÉSICA DE ÁNGULO VARIABLE (PLATE INSTRUMENTS FOR PERI-PROSTHETIC FRACTURE OF VARIABLE ANGLE) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 7853a86800406a22e090fbd4fbc291d0 and manufactured by JOHNSON & JOHNSON MEDTECH COLOMBIA S.A.S.. The device was registered on April 09, 2034.

This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.