BIOFLEX— 510(k) K072321

Substantially Equivalent

Biospine Co., Ltd.

FDA 510(k) clearance K072321 for BIOFLEX, Substantially Equivalent on 2008-03-25. Applicant: Biospine Co., Ltd..

Clearance details

Applicant: Biospine Co., Ltd.
Product code: Code NQP
Advisory panel: Orthopedic
Date received: 2007-08-20
Decision date: 2008-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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