Medtronic, Inc. - FDA 510(k) Cleared Devices
208
Total
207
Cleared
0
Denied
FDA 510(k) cleared devices by Medtronic, Inc. General & Plastic Surgery ✕
13 devices
Cleared
Mar 28, 2024
Emprint Ablation System with Thermosphere Technology (Overall System Name)
General & Plastic Surgery
115d
Cleared
Mar 23, 2023
ClosureFast™ Endovenous Radiofrequency Ablation Catheter
General & Plastic Surgery
122d
Cleared
Apr 08, 2020
TYRX Neuro Absorbable Antibacterial Envelope (Medium), TYRX Neuro Absorbable...
General & Plastic Surgery
198d
Cleared
Mar 27, 2020
TYRX Absorbable Antibacterial Envelope (medium), TYRX Absorbable...
General & Plastic Surgery
206d
Cleared
Jun 07, 2018
TYRX Neuro Absorbable Antibacterial Envelope (medium)
General & Plastic Surgery
142d
Cleared
Apr 24, 2018
TYRX Absorbable Antibacterial Envelope (medium), TYRX Absorbable...
General & Plastic Surgery
111d
Cleared
Oct 04, 2013
THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADES
General & Plastic Surgery
42d
Cleared
Nov 15, 2012
PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR
General & Plastic Surgery
365d
Cleared
Jun 25, 2012
AQUAMANTRYS3 BSC 9.1S
General & Plastic Surgery
56d
Cleared
May 10, 2012
AQUAMANTYS3 9.5 XL BIPOLAR SEALER
General & Plastic Surgery
78d
Cleared
Feb 26, 2010
CARDIOBLATE BIPOLAR RADIOFREQUENCY SURGICAL ABLATION SYSTEM, MODELS 60831,...
General & Plastic Surgery
136d
Cleared
May 07, 2008
U-CLIP UNI-FIRE, MODEL M65
General & Plastic Surgery
21d
Cleared
Feb 28, 2006
CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000
General & Plastic Surgery
13d