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 STREET, N.W., 11TH FL
EAST
WASHINGTON,  DC  20005
Applicant Contact PETER S REICHERTZ
Correspondent
ED. GEISTLICH SOEHNE AG FUR CHEMISCHE INDUSTRIE
1300 I STREET, N.W., 11TH FL
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
-
-