Medartis AG - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
41 devices
Cleared
Dec 18, 2013
APTUS CANNULATED COMPRESSION SCREWS
Orthopedic
36d
Cleared
Apr 27, 2012
APTUS PROXIMAL HUMERUS SYSTEM
Orthopedic
105d
Cleared
Jan 06, 2012
APTUS WRIST ARTHRODESIS PLATES
Orthopedic
162d
Cleared
Dec 15, 2011
APTUS(R) DISTAL HUMERUS SYSTEM
Orthopedic
104d
Cleared
Jun 28, 2011
APTUS FOOT 3.5 SYSTEM
Orthopedic
89d
Cleared
Jun 02, 2011
APTUS CANNULATED COMPRESSION SCREWS
Orthopedic
87d
Cleared
Jan 24, 2011
APTUS ULNA PLATES
Orthopedic
73d
Cleared
Dec 10, 2010
APTUS 1.5 TRILOCK
Orthopedic
98d
Cleared
Sep 23, 2009
APTUS K-WIRE SYSTEM
Orthopedic
79d
Cleared
Jul 13, 2009
APTUS FOOT SYSTEM
Orthopedic
55d
Cleared
Jul 01, 2009
APTUS 2.0/2.3 FOUR CORNER FUSION PLATE
Orthopedic
85d
Cleared
Apr 23, 2009
APTUS 2.0 RADIAL HEAD SYSTEM
Orthopedic
105d
Cleared
Sep 11, 2007
MODUS TRILOCK 2.0/2.3/2.5
Dental
90d
Cleared
Nov 24, 1999
MODUS 2.5 MANDIBULAR RECONSTRUCTION SET
Dental
106d
Cleared
Nov 24, 1999
MODUS 2.5 MANDIBULAR TRAUMA SET
Dental
106d
Cleared
Sep 17, 1999
MODUS SYSTEM SELF-DRILLING SCREWS
Orthopedic
87d