PolyNovo's Synthetic Dermal Scaffold Receives US FDA Clearance

MT Newswires Live
Yesterday

PolyNovo (ASX:PNV) said its synthetic dermal scaffold, NovoSorb MTX (up to 6mm), received US Food and Drug Administration 510(k) clearance, broadening its use in plastic and reconstructive surgery, according to a Wednesday filing with the Australian bourse.

Additionally, NovoSorb MTX (up to 2mm) received approval to be sold and marketed in Australia and approval to be imported into India, the filing said.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Most Discussed

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10