• 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 plate, fixation, bone
510(k) Number K090053
Device Name APTUS 2.0 RADIAL HEAD SYSTEM
Applicant
MEDARTIS AG
11234 EL CAMINO REAL, STE 200
san diego,  CA  92130
Applicant Contact kevin thomas
Correspondent
MEDARTIS AG
11234 EL CAMINO REAL, STE 200
san diego,  CA  92130
Correspondent Contact kevin thomas
Regulation Number888.3030
Classification Product Code
HRS  
Subsequent Product Code
HWC  
Date Received01/08/2009
Decision Date 04/23/2009
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-