510(k) K050377

Device
NBD HEAD SCREW
Applicant
New Business Development, LLC
510(k) number
K050377
Product code
HAW
Decision
Substantially Equivalent (SESE)
Decision date
2005-04-07
Date received
2005-02-15
Regulation
882.4560
Classification name
Neurological Stereotaxic Instrument
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
TIM B LUSBY
Address
605 Industrial Ct. Woodstock GA US 30189 30189

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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