FDA 510(k) Application Details - K051636

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K051636
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	ALTATEC GMBH 520 SOUTH ROCK BLVD. RENO, NV 89502 US Other 510(k) Applications for this Company
Contact	TINA STEFFANIE-OAK Other 510(k) Applications for this Contact
Regulation Number	872.3630   More FDA Info for this Regulation Number
Classification Product Code	NHA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2005
Decision Date	02/17/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review