VENUS FACET SCREW SYSTEM— 510(k) K120340

Name: FDA 510(k) clearance K120340
Creator: U.S. Food and Drug Administration
Published: 2012-10-19

Substantially Equivalent

Apollo Spine, Inc.

FDA 510(k) clearance K120340 for VENUS FACET SCREW SYSTEM, Substantially Equivalent on 2012-10-19. Applicant: Apollo Spine, Inc.. Device class: Unclassified.

Clearance details

Applicant: Apollo Spine, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2012-02-03
Decision date: 2012-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stoughton, MA, 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.