FDA 510(k) Applications Submitted by LAURIMED LLC

FDA 510(k) Number Submission Date Device Name Applicant
K161101 04/19/2016 PolypVac Microdebrider (3.3mm and 4.0mm) LAURIMED LLC
K163247 11/18/2016 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider LAURIMED LLC
K080140 01/22/2008 LAURIMED SPINAL INJECTION SYSTEM LAURIMED LLC
K082194 08/04/2008 LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002 LAURIMED LLC
K133133 09/30/2013 LAURIMED POLYPVAC MICRODEBRIDER LAURIMED LLC
K090815 03/25/2009 PERCUTANEOUS DISCECTOMY SYSTEM LAURIMED LLC
K091818 06/18/2009 LAURIMED SPINAL INJECTION SYSTEM LAURIMED LLC
K083909 12/30/2008 SPINAL INJECTION SYSTEM LAURIMED LLC


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact