• 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 shoulder prosthesis, reverse configuration
510(k) Number K140478
Device Name AEQUALIS REVERSED SHOULDER PROSTHESIS
Applicant
Tornier SAS
161 RUE LAVOISIER
MONTBONNOT SAINT MARTIN,  FR 38330
Applicant Contact MAGALIE HENNEQUIN
Correspondent
Tornier SAS
161 RUE LAVOISIER
MONTBONNOT SAINT MARTIN,  FR 38330
Correspondent Contact MAGALIE HENNEQUIN
Regulation Number888.3660
Classification Product Code
PHX  
Subsequent Product Code
KWS  
Date Received02/26/2014
Decision Date 08/06/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-