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 Appliance, Fixation, Spinal Intervertebral Body
510(k) Number K111132
Device Name GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM
Applicant
GENESYS SPINE
1250 CAPITAL OF TEXAS HWY SO.
BUILDING THREE, SUITE 600
AUSTIN,  TX  78746
Applicant Contact BRIAN J BERGERON
Correspondent
GENESYS SPINE
1250 CAPITAL OF TEXAS HWY SO.
BUILDING THREE, SUITE 600
AUSTIN,  TX  78746
Correspondent Contact BRIAN J BERGERON
Regulation Number888.3060
Classification Product Code
KWQ  
Date Received04/22/2011
Decision Date 12/09/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-