HXB — Probe Class I

FDA Device Classification

Classification Details

Product Code
HXB
Device Class
Class I
Regulation Number
888.4540
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K960539kinetikos medicalDIAO HAND SURGERY SETJuly 23, 1996
K943472cohort medical products groupCOHORT AVB RETRACTOR SYSTEMOctober 20, 1994
K912843flexmedicsFLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBESeptember 24, 1991
K890227kinetic medical productsSURGICAL PROBEJanuary 27, 1989
K873652arthropedicsHOOK PROBE #TM-1376November 2, 1987
K873651arthropedicsBLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375November 2, 1987
K863149bowen and companyBOWEN PROBESeptember 5, 1986
K841971stainless mfg2.5MM & 4MM PROBE K841969-LABELINGJune 19, 1984
K840558conceptSHUTT PRECISION PROBESApril 25, 1984
K810294instraneticsLINE CADDYFebruary 26, 1981
K802951hogan and hartsonI.M PROBESDecember 17, 1980
K802479eder instrument coSURGICAL KNIVES & PROBESOctober 31, 1980
K800729stainless mfgPROBEApril 8, 1980
K800444instrument makarGOLDEN RETRIEVERS OR SILVER RETRIEVERSMarch 5, 1980
K800274acufex microsurgicalACUFEX PROBESFebruary 19, 1980