Matrix Surgical Holdings, LLC/Matrix Surgical USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Matrix Surgical Holdings, LLC/Matrix Surgical USA - FDA 510(k) Cleare...
Recent clearances: OmniPore DUROMAX Surgical Implants
2
Total
2
Cleared
0
Denied
Matrix Surgical Holdings, LLC/Matrix Surgical USA has 2 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 2 cleared submissions from 2014 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Matrix Surgical Holdings, LLC/Matrix Surgical USA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Resources Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Matrix Surgical Holdings, LLC/Matrix Surgical USA
2 devices