Company · US

Twin City Surgical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1987. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GAD	Retractor	1
HXC	Wrench	1
IKK	System, Isokinetic Testing And Evaluation	1
KQW	Goniometer, Nonpowered	1
KTZ	Caliper	1
KWP	Appliance, Fixation, Spinal Interlaminal	1

Decided	510(k)	Device and applicant	Code
Mar 17, 1987	K870767	THE (CROM) TESTER Twin City Surgical, Inc.	KQW
May 27, 1986	K861632	SIMS CHAIR Twin City Surgical, Inc.	IKK
May 27, 1983	K830585	ANVIL RETRACTOR Twin City Surgical, Inc.	GAD
Mar 19, 1982	K820660	A HOOK DRIVER Twin City Surgical, Inc.	KWP
Mar 19, 1982	K820659	A CALIPER Twin City Surgical, Inc.	KTZ
Nov 24, 1981	K813067	SPINAL WRENCH Twin City Surgical, Inc.	HXC

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