Company · US

Stuart

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1990. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
KWQ	Appliance, Fixation, Spinal Intervertebral Body	2
EZX	Mesh, Surgical, Metal	1
JDN	Implant, Fixation Device, Spinal	1
KWP	Appliance, Fixation, Spinal Interlaminal	1

Decided	510(k)	Device and applicant	Code
Jun 21, 1990	K897141	SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO Stuart	JDN
Mar 16, 1989	K890601	STUART TITANIUM SURGICAL MESH Stuart	EZX
Jun 28, 1985	K851414	SEGMENTAL SPINAL RODS Stuart	KWQ
Feb 13, 1985	K843445	SACRAL BAR Stuart	KWP
Mar 11, 1982	K820034	ANTERIOR DISTRACTION SYSTEM Stuart	KWQ

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.