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Instratek, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K131620	JONES-FX FRACTURE SYSTEM	HWC	2013-07-25	View
510(k)	K120493	MINI CANNULATED HEADED AND HEADLESS SCREW SET	HWC	2012-05-17	View
510(k)	K111032	CMC CABLE FIX	HTN	2011-08-31	View
510(k)	K091763	MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000	HTN	2009-08-14	View
510(k)	K082384	HAV-LOK BUNION CORRECTION SYSTEM	HTN	2008-12-08	View
510(k)	K080280	SUB-TALAR LOK, MODEL 7-11 MM	HWC	2008-03-14	View
510(k)	K940230	ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS	HRX	1994-12-12	View
510(k)	K925083	ENDOTRAK SYSTEM	HRX	1993-04-27	View
510(k)	K922391	ENDOSCOPIC CARPAL TUNNEL INSTRUMENTS	HRX	1992-08-18	View

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