FDA.reportPublic FDA data

510(k) K771020

Device
SPINAL SURGERY FRAME
Applicant
Orthopedic Systems, Inc.
510(k) number
K771020
Product code
JEB
Decision
Substantially Equivalent (SESE)
Decision date
1977-06-17
Date received
1977-06-06
Regulation
878.4950
Classification name
Table, Surgical With Orthopedic Accessories, Manual
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
N

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 JEB#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K905816ORTHOVISION TABLEAmerican Sterilizer Co.1991-03-06
K900405SCHOLTEN FRAMEScholten Surgical Instruments, Inc.1990-03-01
K891917ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.1989-05-26
K891387WILLIAMS BELT & BOOTArthro-Medic, Inc.1989-05-23
K881101K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.1988-04-06
K880263OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, Inc.1988-03-15
K873273ORTHOPAEDIC TABLE 1420Stierlen-Maquet AG1987-09-17
K873274PLASTER TABLE 1418Stierlen-Maquet AG1987-09-17
K873275EXTENSION TABLE 1417Stierlen-Maquet AG1987-09-17
K873276EXTENSION DEVICE 1416Stierlen-Maquet AG1987-09-17
K781082CAST BLOCKOrthopedic Equipment Co., Inc.1978-07-07
K772321ARTHROSTRESSMtd, Inc.1978-01-03