DGAP-Ad-hoc: CO.DON AG / Key word(s): Regulatory Approval
CO.DON AG: EU approval of the articular cartilage product by the European Commission

12-Jul-2017 / 16:09 CET/CEST
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CO.DON AG (ISIN: DE DE000A1K0227)

EU approval of the articular cartilage product by the European Commission

Berlin / Teltow, 12 July 2017 - Today, CO.DON AG received the Commission's implementing decision of 10.07.2017 on the granting of marketing authorization for the human pharmaceutical product "Spherox - Spheroids from human autologous matrix-associated chondrocytes", pursuant to Regulation (EC ) No 726/2004 of the European Parliament and of the Council. The approved indication is the repair of symptomatic joint cartilage defects of the ICRS grade III or IV of the femoral condylar and the patella of the knee with defects of up to 10 cm2 in adults.

Further Informationen:

Matthias Mei?ner, M.A.

Investor Relations

ir@codon.de

12-Jul-2017 CET/CEST The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.
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Language: English
Company: CO.DON AG
Warthestra?e 21
14513 Teltow
Germany
Phone: 03328 43460
Fax: 03328 434643
E-mail: info@codon.de
Internet: www.codon.de
ISIN: DE000A1K0227
WKN: A1K022
Listed: Regulated Market in Frankfurt (General Standard); Regulated Unofficial Market in Berlin, Dusseldorf, Hamburg, Stuttgart, Tradegate Exchange

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