Bone matrix implant, artificial
Country: Australia
Language: English
Source: Department of Health (Therapeutic Goods Administration)
Public Assessment Report
(PAR)
10-11-2017
Some documents for this product are not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain them.
Send request.
Send request.
Available from:
Zimmer Biomet Pty Ltd
Class:
Class IIb
Manufactured by:
Biomet Trauma 56 East Bell Drive, Warsaw, IN, 46581 United States Of America
Therapeutic area:
17751 - Bone matrix implant, synthetic
Therapeutic indications:
Titanium alloy porous metal osteoconductive matrix for use as a reconstructive wedge for internal bone fixation for bone structures, fusions or osteotomies, such as open wedge osteotomies; Evans lengthening osteotomies; metatarsal/cuneiform arthrodesis.
Authorization status:
A
Authorization date:
2013-12-12
