Atlas FDA

Zimmer Spine, Inc.

14 FDA 510(k) clearances · PMA applicant

Sort:Newest firstOldest first

◉ Watch Zimmer Spine, Inc.

RecordFirmDate
BAK VISTA INTERBODY FUSION CAGE (P950002/S014)Zimmer Spine, Inc.2004-07-01
VISTA LORDOTIC INTERBODY FUSION CAGE (P950002/S013)Zimmer Spine, Inc.2004-01-29
BAK VISTA INTERBODY FUSION CAGE (P950002/S012)Zimmer Spine, Inc.2003-10-31
BAK VISTA INTERBODY FUSION DEVICE (P950002/S011)Zimmer Spine, Inc.2003-07-08
BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE (P950002/S007)Zimmer Spine, Inc.2002-05-01
BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM (P950002/S009)Zimmer Spine, Inc.2001-04-03
BAK/L INTERBODY FUSION SYSTEM (P950002/S008)Zimmer Spine, Inc.1999-12-20
BAK INTERBODY FUSION SYSTEM (P950002/S006)Zimmer Spine, Inc.1998-05-12
BAK INTERBODY FUSION SYSTEM (P950002/S005)Zimmer Spine, Inc.1998-02-06
BAK INTERBODY FUSION SYSTEM (P950002/S003)Zimmer Spine, Inc.1997-10-15
BAK INTERBODY FUSION SYSTEM (P950002/S001)Zimmer Spine, Inc.1997-07-22
BAK INTERBODY FUSION SYSTEM (P950002/S004)Zimmer Spine, Inc.1997-06-30
BAK INTERBODY FUSION SYSTEM (P950002/S002)Zimmer Spine, Inc.1997-05-09
BAK INTERBODY FUSION SYSTEM (P950002)Zimmer Spine, Inc.1996-09-20

Track Zimmer Spine, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.