SPINE ALIGN— 510(k) K801952

Substantially Equivalent

B.H. Richardson, D.C.

FDA 510(k) clearance K801952 for SPINE ALIGN, Substantially Equivalent on 1980-09-16. Applicant: B.H. Richardson, D.C.. Device class: 2.

Clearance details

Applicant: B.H. Richardson, D.C.
Product code: Code KYI
Device class: Class 2
Regulation: 21 CFR 888.3770
Advisory panel: Orthopedic
Date received: 1980-08-18
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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