Depuy Mitek - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Depuy Mitek has 13 FDA 510(k) cleared medical devices. Based in Norwood, US.
Latest FDA clearance: Feb 2025. Active since 2004. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy Mitek Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Depuy Mitek
13 devices
Cleared
Feb 05, 2025
GRYPHON™ X Anchor
Orthopedic
57d
Cleared
Sep 11, 2024
HEALIX ADVANCE Knotless anchors
Orthopedic
152d
Cleared
Mar 15, 2024
MILAGRO Interference Screw
Orthopedic
30d
Cleared
Apr 03, 2015
VAPR Tripolar Suction Electrode
General & Plastic Surgery
119d
Cleared
May 11, 2012
HEALIX ADVANCE PEEK ANCHOR
Orthopedic
87d
Cleared
Apr 23, 2008
DOUBLE ARMED MENISCAL NEEDLES WITH SIZE #2-0 ORTHOCORD, MENISCAL NEEDLE WITH...
General & Plastic Surgery
22d
Cleared
Jun 06, 2006
FASTIN RC ANCHOR
Orthopedic
85d
Cleared
Dec 10, 2004
BLUE ORTHOCORD SUTURE
General & Plastic Surgery
10d
Cleared
May 28, 2004
SUPER QUICKANCHOR PLUS
Orthopedic
29d
Cleared
May 28, 2004
PANALOK RC QUICKANCHOR PLUS, MODEL 212130, 212730
Orthopedic
29d
Cleared
May 13, 2004
BIOKNOTLESS RC ANCHOR
Orthopedic
20d
Cleared
May 07, 2004
PANALOK RC LOOP ANCHOR
Orthopedic
14d