Depuy Mitek, A Johnson & Johnson Company - FDA 510(k) Cleared Devices
Recent clearances: Milagro / Milagro Advance Interference Screw, 4.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture, 5.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture, 6.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture,, VAPR ARCTIC SUCTION ELECTRODE
58
Total
58
Cleared
0
Denied
FDA 510(k) Regulatory Record - Depuy Mitek, A Johnson & Johnson Company General & Plastic Surgery ✕
9 devices
Cleared
Aug 05, 2014
VAPR ARCTIC SUCTION ELECTRODE
General & Plastic Surgery
119d
Cleared
Nov 05, 2012
VAPR P50 SUCTION ELECTRODE VAPR S90 SUCTION ELECTRODE VAPR P50 SUCTION...
General & Plastic Surgery
88d
Cleared
Apr 06, 2012
SIDE EFFECT WITH HAND CONTROLS, HOOK ELECTRODE WITH HAND CONTROLS, 2.3 WEDGE...
General & Plastic Surgery
85d
Cleared
Feb 27, 2012
VAPR VUE GENERATOR, VAPR 3 ELECTROSURGICAL SYSTEM, VAPR II ELECTROSURGICAL...
General & Plastic Surgery
88d
Cleared
Jun 18, 2010
VAPR VUE RADIOFREQUENCY SYSTEM ,MODEL 225024, VPR VUE WIRELESS FOOTSWITCH,...
General & Plastic Surgery
105d
Cleared
Dec 19, 2008
3.5 MM SIDE EFFECT ELECTRODE WITH INTEGRATED HANDPIECE, MODEL 227301, 3.5 MM...
General & Plastic Surgery
99d
Cleared
Apr 08, 2005
LUPINE LOOP
General & Plastic Surgery
14d
Cleared
Sep 28, 2004
PASSING NEEDLE WITH ETHIBOND, PANACRYL OR ORTHOCORD SUTURE
General & Plastic Surgery
41d
Cleared
Aug 03, 2004
PASSING NEEDLE WITH ETHIBOND, PANACRYL OR ORTHOCORD SUTURE
General & Plastic Surgery
28d