FDA 510(k) Applications Submitted by OSTEOMED CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K151021 04/16/2015 OsteoMed Cannulated Screw System OSTEOMED CORP.
K974785 12/22/1997 AUTO-DRIVE BONE SCREW OSTEOMED CORP.
K971692 05/07/1997 OSTEOPOWER SYSTEM AND ACCESSORIES OSTEOMED CORP.
K010783 03/15/2001 2.0/2.4 CANNULATED SCREW SYSTEM OSTEOMED CORP.
K010964 03/30/2001 AUTO-DRIVE LAG SCREW SYSTEM OSTEOMED CORP.
K021618 05/16/2002 OSA RIGID INTERNAL FIXATION SYSTEM OSTEOMED CORP.
K022277 07/15/2002 OSTEOMED CRANIAL FLAP FIXATION SYSTEM OSTEOMED CORP.
K012486 08/02/2001 OSTEOMED BIORESORBABLE FIXATION SYSTEM OSTEOMED CORP.
K022886 08/30/2002 METATARSOPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM OSTEOMED CORP.
K022887 08/30/2002 INTERPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM OSTEOMED CORP.
K023260 09/30/2002 1.2MM OSTEOMED AUTO-DRIVE SCREW SYSTEM OSTEOMED CORP.
K013618 11/05/2001 INTRAORAL MANDIBULAR DISTRACTION SYSTEM OSTEOMED CORP.
K961418 04/12/1996 OSTEOMED MSS OSTEOMED CORP.
K962774 07/16/1996 OSTEOMED QUICKFIX OSTEOMED CORP.
K963394 08/28/1996 OSTEOMED TRAM OSTEOMED CORP.
K990944 03/22/1999 OSTEOMED INTRAORAL DISTRACTION SYSTEM OSTEOMED CORP.


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