Arthrex Quickset - Bone matrix implant, synthetic

País: Austrália

Língua: inglês

Origem: Department of Health (Therapeutic Goods Administration)

Disponível em:

Arthrex Australia Pty Ltd

Classe:

Class III

Fabricado por:

Graftys Eiffel Park Bat D415 rue Claude Nicolas Ledoux Pole, AIX EN Provence, dActivities dAix en Provence, Cedex 3, 13854 France

Área terapêutica:

17751 - Bone matrix implant, synthetic

Indicações terapêuticas:

Arthrex Quickset device is an injectable self-hardening macroporous calcium phosphate bone void filler. The procedure pack includes Arthrex Quickset and a sterile cannula which is connected to the syringe tip and used to direct the Quickset into the appropriate site. Arthrex Quickset is intended for filling or reinforcing bony voids or defects of the skeletal system that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. These products provide a bone void filler that resorbs and is replaced with bone during the healing process.

Status de autorização:

A

Data de autorização:

2016-01-22