FDA 510(k) Applications Submitted by ACROMED CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K972718	07/21/1997	M-2 ANTERIOR PLATE SYSTEM	ACROMED CORP.
K974757	12/19/1997	KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS	ACROMED CORP.
K953978	08/23/1995	ANTERIOR DYNAMIZED SYSTEM	ACROMED CORP.
K952236	05/12/1995	ISOLA SYSTEM	ACROMED CORP.
K970950	03/14/1997	EASY ROD	ACROMED CORP.
K981274	04/08/1998	ACROMED TIMX PLATE BASED LOW BACK SYSTEM	ACROMED CORP.
K981714	05/15/1998	TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM	ACROMED CORP.
K970955	03/17/1997	ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM	ACROMED CORP.
K970462	02/06/1997	ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM	ACROMED CORP.
K980228	01/22/1998	UNIVERSITY PLATE ANTERIOR SYSTEM	ACROMED CORP.
K980485	02/09/1998	ISOLA SPINAL SYSTEM	ACROMED CORP.
K981113	03/27/1998	PEDIATRIC PRC	ACROMED CORP.
K971248	04/03/1997	KANEDA SR ANTERIOR SPINAL SYSTEM	ACROMED CORP.
K962645	07/08/1996	ISOLA TWISTER CONNECTOR	ACROMED CORP.
K962984	08/01/1996	ISOLA PEDIATRIC COMPONENTS	ACROMED CORP.
K963639	09/12/1996	ACROMED PEDICLE SCREW	ACROMED CORP.
K964007	10/07/1996	ACROMED CABLE/WIRE PEDICLE SCREW	ACROMED CORP.
K965046	12/18/1996	ISOLA TWISTER CONNECTOR	ACROMED CORP.
K965102	12/20/1996	ACROMED PEDICLE SCREW	ACROMED CORP.