Cedar Surgical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K873692RAYLOR(TM) DRILL STOPDecember 17, 1987
K872281RAYLOR FUSION FUNNELNovember 2, 1987
K873690CEDAR(TM) PELVIC CUSHIONOctober 26, 1987
K873691CEDAR(TM) RETRACTOR RINGSeptember 28, 1987
K864425RAYLOR(TM) DISSECTING HOOKDecember 12, 1986
K864421RAYLOR(TM) PERIOSTEAL ELEVATORSNovember 26, 1986
K864426RAYLOR(TM) DEPTH GAUGENovember 26, 1986
K864424RAYLOR(TM) PROTECTIVE RETRACTORNovember 26, 1986
K864423RAYLOR(TM) OSTEOTOMESNovember 24, 1986
K864422RAYLOR(TM) MALLETNovember 24, 1986
K863415RAYLOR BONE IMPACTORSSeptember 24, 1986
K863416RAYLOR MINI-PROBESeptember 24, 1986
K853799NEUROSURGICAL HEADRESTOctober 7, 1985
K853798BONE IMPACTORSOctober 7, 1985
K853797KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOROctober 7, 1985
K853796RAYLOR RETRACTORSOctober 7, 1985
K853800UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITTOctober 7, 1985