510(k) K802598

Device: CARBIDE CUTTING INSTRUMENT/INTRAARTICU
Applicant: The Anspach Effort, Inc.
510(k) number: K802598
Product code: HTT
Decision: Substantially Equivalent (SESE)
Decision date: 1980-11-19
Date received: 1980-10-21
Regulation: 888.4540
Classification name: Burr, Orthopedic
Medical specialty: Orthopedic
Review panel: Orthopedic
Device class: 1
Clearance type: Traditional
Third party reviewed: No

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 HTT#

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K862529	HALL STERILE BUR	Hall Surgical, Division of Zimmer, Inc.	1986-07-15
K821695	MICRO-AIRE REPLAC. DRILL BURS FOR ZIMMER	Micro-Aire Surgical Instruments, Inc.	1982-07-20
K760236	BUR, SURGICAL CARBIDE	Cutter Laboratories, Inc.	1976-07-26