FDA 510(k) Applications Submitted by DREW WEAVER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990378	02/08/1999	STATVIEW SYSTEM	DATA CRITICAL CORP.
K251052	04/03/2025	Trivicta« Hip Stem	Ortho Development Corp.
K161080	04/18/2016	Escalade Legend Acetabular Shell	ORTHO DEVELOPMENT CORPORATION
K171249	04/28/2017	EntradaÖ hip stem	Ortho Development Corporation
K152169	08/04/2015	Balanced Knee System TriMax CR Femoral Component and E-Vitalize CR and UC Tibial Inserts	ORTHO DEVELOPMENT CORPORATION
K992848	08/24/1999	ALARMVIEW SYSTEM	DATA CRITICAL CORP.
K242833	09/19/2024	Legend« Acetabular Shell	Ortho Development Corp.
K233093	09/26/2023	Balanced Knee« System TriMax PS Plus Tibial Insert	Ortho Development Corporation
K242984	09/26/2024	BKS Revision System	Ortho Development Corp.
K153216	11/05/2015	Alpine Cemented Hip System	ORTHO DEVELOPMENT CORPORATION
K233758	11/24/2023	TrivictaÖ Hip Stem	Ortho Development Corp.
K173951	12/27/2017	Legend Acetabular Liners	Ortho Development Corporation
K965054	12/18/1996	PENCIL	MEGADYNE MEDICAL PRODUCTS, INC.