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 Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
510(k) Number K100555
Device Name APEX-LNK ACETABULAR INSERT, E, APEX-LNK ACETABULAR INSERT, F, APEX-LNK
Applicant
OMNI LIFE SCIENCE, INC.
50 O'CONNELL WAY
EAST TAUNTON,  MA  02718
Applicant Contact RADHIKA PONDICHERRY
Correspondent
OMNI LIFE SCIENCE, INC.
50 O'CONNELL WAY
EAST TAUNTON,  MA  02718
Correspondent Contact RADHIKA PONDICHERRY
Regulation Number888.3358
Classification Product Code
LPH  
Subsequent Product Codes
LZO   MEH  
Date Received03/01/2010
Decision Date 03/29/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-