FDA.reportPublic FDA data

510(k) K873066

Device
ACROMED SCREW DRIVER
Applicant
BUCKMAN CO., INC.
510(k) number
K873066
Product code
HXX  
Decision
Substantially Equivalent (SESE)
Decision date
1987-09-02
Date received
1987-08-05
Regulation
888.4540
Classification name
Screwdriver
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
DAVID W SCHLERF
Address
921 Calle Verde Martinez CA US 94553 94553

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HXX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K901166DALTON TECHNOLOGY FLEXIBLE SCREWDRIVERDalton Technology, Inc.1990-06-13
K872389PRECISION SCREW DRIVER SETMed-Tool, Inc.1987-07-15
K8626892.5MM HEX DRIVER/CURVE PASSER/BONE PUNCH/RASPW. L. Gore & Associates, Inc.1986-09-02

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases