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Smith & Nephew, Inc., Orthopaedic Div.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K991538	OPERA CUPFLANGED ACETABULAR COMPONENTS	JDI	1999-06-03	View
510(k)	K970635	TITANIUM SPINAL ROD SYSTEM	KWQ	1997-08-14	View
510(k)	K971414	ZIRCONIA PROZYR CERAMIC 12/14 GLOBAL TAPER (GT) FEMORAL HEADS	LZO	1997-07-16	View
510(k)	K970748	TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEM	KTT	1997-05-09	View
510(k)	K970751	HEIDELBERG EXTERNAL FIXATOR	JDW	1997-04-16	View
510(k)	K970713	COMPASS UNIVERSAL HINGE	JDW	1997-04-03	View
510(k)	K970337	HA GLOBAL TAPER (GT) TAPERED HIP STEM	MEH	1997-02-28	View
510(k)	K970351	GLOBAL TAPER SPECTRON HIP STEMS	JDI	1997-02-28	View
510(k)	K963255	PROFIX PLUS TIBIAL INSERT, PROFIX PS PLUS TIBIAL INSERT, PROFIX P/S TIBIAL INSERT	JWH	1997-01-02	View
510(k)	K962784	ULTIUM SPINAL PLATING SYSTEM	MNH	1996-10-02	View

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