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 Barrier, Animal Source, Intraoral
510(k) Number K102531
Device Name MUCOGRAFT
Applicant
Ed. Geistlich Soehne AG Fur Chemische Industrie
1300 I St., NW, 11th Floor
East
Washington,  DC  20005
Applicant Contact PETER S REICHERTZ
Correspondent
Ed. Geistlich Soehne AG Fur Chemische Industrie
1300 I St., NW, 11th Floor
East
Washington,  DC  20005
Correspondent Contact PETER S REICHERTZ
Regulation Number872.3930
Classification Product Code
NPL  
Date Received09/03/2010
Decision Date 11/17/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-