Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Mesh, Surgical, Polymeric
510(k) Number K110110
Device Name ATRIUM CENTRILFX MESH
Applicant
Atrium Medical Corporation
5 Wentworth Dr.
Hudson,  NH  03051
Applicant Contact RAYMOND J KELLY
Correspondent
Atrium Medical Corporation
5 Wentworth Dr.
Hudson,  NH  03051
Correspondent Contact RAYMOND J KELLY
Regulation Number878.3300
Classification Product Code
FTL  
Date Received01/14/2011
Decision Date 02/15/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-