FDA 510(k) Applications Submitted by CERAMED CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960348	01/25/1996	OSTEOGRAF/N-300 HYDROXYLAPATITE	CERAMED CORP.
K960349	01/25/1996	PERMARIDGE HYDROXYLAPATITE MATRIX	CERAMED CORP.
K960353	01/25/1996	OSTEOGRAF/LD-300 HYDROXYLAPATITE	CERAMED CORP.
K960354	01/25/1996	PERMAMESH-D HYDROXYLAPATITE MATRIX	CERAMED CORP.
K960361	01/25/1996	PERMAMESH-D HYDROXYLAPATITE MATRIX	CERAMED CORP.
K960362	01/25/1996	PERMAMESH HYDROXYLAPATITE MATRIX	CERAMED CORP.
K960368	01/25/1996	OSTEOGRAFT/N-700 HYDROXYLAPTITE	CERAMED CORP.
K962786	07/17/1996	OSTEOGRAF STAINLESS STEEL SYRING	CERAMED CORP.
K962838	07/22/1996	PERMARIDGE SYRINGE	CERAMED CORP.
K954631	10/06/1995	OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE	CERAMED CORP.