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 Filler, Bone Void, Calcium Compound
510(k) Number K082793
Device Name INTERGRO DBM
Applicant
Biomet Spine
181 Technology Dr.
Irvine,  CA  92618
Applicant Contact KATHLEEN IDEO
Correspondent
Biomet Spine
181 Technology Dr.
Irvine,  CA  92618
Correspondent Contact KATHLEEN IDEO
Regulation Number888.3045
Classification Product Code
MQV  
Subsequent Product Codes
GXP   MBP  
Date Received09/23/2008
Decision Date 04/02/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-