FIDJI LARGE CEMENT RESTRICTOR— 510(k) K030871

Unknown

Spine Next SA

FDA 510(k) clearance K030871 for FIDJI LARGE CEMENT RESTRICTOR, Unknown on 2003-12-22. Applicant: Spine Next SA. Device class: 2.

Clearance details

Applicant: Spine Next SA
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-03-19
Decision date: 2003-12-22
Decision: Unknown
Clearance type: Traditional
Location: Queenstown, MD, US

Download summary PDF View on FDA.gov ↗

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K060247 — LIFE SPINE CEMENT RESTRICTOR2006-05-11
K060132 — SPINAL USA CEMENT RESTRICTOR SYSTEM2006-03-16

More clearances from Spine Next SA

K030767 — FIDJI SMALL CEMENT RESTRICTOR2003-12-22
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Data sourced from openFDA. This site is unofficial and independent of the FDA.