FDA 510(k) Applications Submitted by PIONEER SURGICAL TECHNOLOGY, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110692	03/11/2011	STREAMLINE TL SPINAL SYSTEM	PIONEER SURGICAL TECHNOLOGY, INC.
K112496	08/29/2011	PIONEER CROSSFUSE II IBF/VBR SYSTEM	PIONEER SURGICAL TECHNOLOGY, INC.
K112757	09/22/2011	PIONEER POSTERIOR CERVICO THORACIC SYSTEM	PIONEER SURGICAL TECHNOLOGY, INC.
K102903	09/30/2010	PIONEER CANNULATED SCREW SYSTEM	PIONEER SURGICAL TECHNOLOGY, INC.
K111944	07/08/2011	NB3D BONE VOID FILLER	PIONEER SURGICAL TECHNOLOGY, INC.
K211408	05/06/2021	CervAlign« Anterior Cervical Plate System	Pioneer Surgical Technology, Inc.
K192396	09/03/2019	Streamline MIS Spinal Fixation System	Pioneer Surgical Technology, Inc.
K130427	02/20/2013	PIONEER ASPECT ANTERIOR CERVICAL PLATE SYSTEM	PIONEER SURGICAL TECHNOLOGY, INC.