LIFE SPINE CEMENT RESTRICTOR— 510(k) K060247

Unknown

Life Spine

FDA 510(k) clearance K060247 for LIFE SPINE CEMENT RESTRICTOR, Unknown on 2006-05-11. Applicant: Life Spine. Device class: 2.

Clearance details

Applicant: Life Spine
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2006-01-31
Decision date: 2006-05-11
Decision: Unknown
Clearance type: Traditional
Location: Hoffman Estates, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JDK

K210062 — Mectaplug PE II2021-04-08
K061465 — KMI CEMENT RESTRICTOR IMPLANT2006-10-05
K061698 — MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR2006-07-12
K060132 — SPINAL USA CEMENT RESTRICTOR SYSTEM2006-03-16
K051371 — INTERBODY INNOVATIONS CEMENT RESTRICTOR2005-12-06

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K141905 — PRO-LINK WEDGE SYSTEM2014-09-26
K133717 — LONGBOW SPACER SYSTEM2014-09-19

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