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 K014107
Device Name ENDIUS CERVICAL PLATE SYSTEM
Applicant
Endius, Inc.
23 W. Bacon St.
Plainville,  MA  02762
Applicant Contact GENE DIPOTO
Correspondent
Endius, Inc.
23 W. Bacon St.
Plainville,  MA  02762
Correspondent Contact GENE DIPOTO
Regulation Number888.3060
Classification Product Code
KWQ  
Date Received12/13/2001
Decision Date 02/13/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-