510(k) K834384

Device: Modular Extremity Casting Support
Applicant: BUCKMAN CO., INC.
510(k) number: K834384
Product code: LGG
Decision: Substantially Equivalent (SESE)
Decision date: 1984-01-30
Date received: 1983-12-14
Regulation: 888.5980
Classification name: Instrument, Cast Application/Removal, Manual
Medical specialty: Orthopedic
Review panel: Orthopedic
Device class: 1
Clearance type: Traditional
Third party reviewed: No

Applicant Contact#

Address: 803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LGG#

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K870100	PLASTER STAND	Orthopedic Systems, Inc.	1987-01-28
K851786	27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF	Artiberia	1985-07-09