Linvatec Corp. - FDA 510(k) Cleared Devices

Cleared Feb 25, 2009

EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR,...

K083281 · GEI

General & Plastic Surgery · 110d

Cleared May 17, 2005

ADVANCED TURBO DRIVE SYSTEM

K050519 · GEY

General & Plastic Surgery · 77d

Cleared Dec 15, 2003

TRIDENT RESECTION ABLATOR

K033748 · GEI

General & Plastic Surgery · 14d

Cleared Jun 04, 2003

3-CCD DIGITAL CAMERA SYSTEM

K031098 · GCJ

General & Plastic Surgery · 58d

Cleared Jun 03, 2003

ULTRABLATOR ELECTRODE

K030720 · GEI

General & Plastic Surgery · 88d

Cleared Apr 04, 2002

RESECTION ABLATOR

K013369 · GEI

General & Plastic Surgery · 175d

Cleared Oct 19, 2001

POWERPRO BATTERY SYSTEM

K012320 · HAB

General & Plastic Surgery · 88d

Cleared Feb 10, 2000

ULTRABLATOR ELECTRODE

K993885 · JOS

General & Plastic Surgery · 86d

Cleared Aug 20, 1999

CAPSULAR SHRINKAGE ELECTRODE

K991830 · JOS

General & Plastic Surgery · 84d

Cleared Apr 27, 1995

ELECTRODES

K944992 · JOS

General & Plastic Surgery · 197d

Cleared Nov 17, 1994

SENSATEC ENDOSCOPIC INSTRUMENTS

K942080 · GEI

General & Plastic Surgery · 202d

Cleared Nov 14, 1994

BI-TEC ENDOSCOPIC BIPOLAR INSTRUMENTS

K942077 · GEI

General & Plastic Surgery · 199d