FLEXION DISTRACTION TABLE— 510(k) K933622

Substantially Equivalent

Spinalight, Inc.

FDA 510(k) clearance K933622 for FLEXION DISTRACTION TABLE, Substantially Equivalent on 1994-01-07. Applicant: Spinalight, Inc..

Clearance details

Applicant: Spinalight, Inc.
Product code: Code INQ
Advisory panel: Physical Medicine
Date received: 1993-07-19
Decision date: 1994-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodstock, GA, US

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