Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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