DeviceClearance

TORQUE INSTRUMENT, MODEL 8500— 510(k) K001476

Substantially Equivalent

Spinalight, Inc.

FDA 510(k) clearance K001476 for TORQUE INSTRUMENT, MODEL 8500, Substantially Equivalent on 2000-08-04. Applicant: Spinalight, Inc..

Clearance details

Applicant
Spinalight, Inc.
Product code
Code LXM
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Kennesaw, GA, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.