Acra Cut, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K032970ACRA-CUT XPRESS 120December 8, 2003
K944311ACRA-CUTNovember 18, 1994
K911812ACRA-CUT WIRE PASS DRILLSeptember 10, 1991
K911819ACRA-CUT NEUROLOGICAL SURGICAL DEVICE-POWEREDSeptember 10, 1991
K910226DURAL DISSECTORSFebruary 12, 1991
K910225BONE PAD REMOVERFebruary 12, 1991
K892866AUTOMATIC CRANIAL DRILL (PERFORATOR)June 15, 1989
K833266ACRA-CUTDecember 29, 1983