FDA 510(k) Applications Submitted by DIANE DAVIS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K230328	02/06/2023	Speedboat Flush SB1 Instrument	Creo Medical Ltd
K961122	03/21/1996	STRYKER KNIFELIGHT	STRYKER INSTRUMENTS
K961970	05/20/1996	COMMAND 2 MICOELECTRIC SURGICAL SYSTEM	STRYKER CORP.
K242061	07/15/2024	Reusable Interface Cable 1.5 m (PRD-IFC-002)	Creo Medical Ltd
K962800	07/18/1996	STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES	STRYKER INSTRUMENTS
K242774	09/13/2024	SpydrBlade Flex Instrument (PRD-RG1-001)	Creo Medical Ltd
K242983	09/26/2024	CROMA Electrosurgical Generator (PRD-EMR-050)	Creo Medical Ltd