FDA 510(k) Application Details - K895462

Device Classification Name Implant, Endosseous, Root-Form

  More FDA Info for this Device
510(K) Number K895462
Device Name Implant, Endosseous, Root-Form
Applicant COLLAGEN CORP.
2500 FABER PLACE
PALO ALTO, CA US
Other 510(k) Applications for this Company
Contact CINDY DOMECUS
Other 510(k) Applications for this Contact
Regulation Number 872.3640

  More FDA Info for this Regulation Number
Classification Product Code DZE
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 09/06/1989
Decision Date 04/04/1990
Decision SE - Substantially Equivalent
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact