Product code HXB— Orthopedic

FDA has cleared 15 devices under product code HXB between 1980 and 1996, filed by 13 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19961 clearance
• 19941 clearance
• 19911 clearance
• 19891 clearance
• 19872 clearances
• 19861 clearance
• 19842 clearances
• 19811 clearance
• 19805 clearances

• Stainless Mfg., Inc.2 clearances
• Arthropedics, Inc.2 clearances
• Kinetikos Medical, Inc.1 clearance
• Kinetic Medical Products1 clearance
• Instrument Makar, Inc.1 clearance
• Instranetics, Inc.1 clearance
• Hogan & Hartson1 clearance
• Flexmedics1 clearance
• Eder Instrument Co, Inc.1 clearance
• Concept, Inc.1 clearance

• K960539 — DIAO HAND SURGERY SETKinetikos Medical, Inc.·1996-07-23
• K943472 — COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.·1994-10-20
• K912843 — FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedics·1991-09-24
• K890227 — SURGICAL PROBEKinetic Medical Products·1989-01-27
• K873651 — BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.·1987-11-02
• K873652 — HOOK PROBE #TM-1376Arthropedics, Inc.·1987-11-02
• K863149 — BOWEN PROBEBowen & Company, Inc.·1986-09-05
• K841971 — 2.5MM & 4MM PROBE K841969-LABELINGStainless Mfg., Inc.·1984-06-19
• K840558 — SHUTT PRECISION PROBESConcept, Inc.·1984-04-25
• K810294 — LINE CADDYInstranetics, Inc.·1981-02-26
• K802951 — I.M PROBESHogan & Hartson·1980-12-17
• K802479 — SURGICAL KNIVES & PROBESEder Instrument Co, Inc.·1980-10-31
• K800729 — PROBEStainless Mfg., Inc.·1980-04-08
• K800444 — GOLDEN RETRIEVERS OR SILVER RETRIEVERSInstrument Makar, Inc.·1980-03-05
• K800274 — ACUFEX PROBESAcufex Microsurgical, Inc.·1980-02-19