INION SPINAL GRAFT CONTAINMENT SYSTEM— 510(k) K071810

Unknown

Inion , Ltd.

FDA 510(k) clearance K071810 for INION SPINAL GRAFT CONTAINMENT SYSTEM, Unknown on 2008-07-11. Applicant: Inion , Ltd.. Device class: 2.

Clearance details

Applicant: Inion , Ltd.
Product code: Code OJB
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2007-07-02
Decision date: 2008-07-11
Decision: Unknown
Clearance type: Traditional
Location: Tampere, FI

Download summary PDF View on FDA.gov ↗

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