• 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 bone grafting material, synthetic
510(k) Number K083858
Device Name BOND BONE
Applicant
AUGMA BIOMATERIALS, LTD.
11234 EL CAMINO REAL
SUITE 200
san diego,  CA  92130
Applicant Contact david j collette
Correspondent
AUGMA BIOMATERIALS, LTD.
11234 EL CAMINO REAL
SUITE 200
san diego,  CA  92130
Correspondent Contact david j collette
Regulation Number872.3930
Classification Product Code
LYC  
Date Received12/24/2008
Decision Date 03/17/2009
Decision substantially equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-