SPINAL SPHERE SYSTEM— 510(k) K073274

Unknown

Life Spine

FDA 510(k) clearance K073274 for SPINAL SPHERE SYSTEM, Unknown on 2008-03-17. Applicant: Life Spine. Device class: 3.

Clearance details

Applicant: Life Spine
Product code: Code NVR
Device class: Class 3
Advisory panel: Unknown
Date received: 2007-11-21
Decision date: 2008-03-17
Decision: Unknown
Clearance type: Traditional
Location: Hoffman Estates, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NVR

K073105 — PEEK SPINAL SPHERES2008-01-03
K062992 — SPINAL SPHERES2007-07-27
K063139 — SPINAL STABILIZING SPHERE SYSTEM2007-04-04
K060415 — MODIFICATION TO: SATELLITE SPINAL SYSTEM2007-01-05
K051320 — SATELLITE SPINAL SYSTEM2005-09-09

More clearances from Life Spine

K182470 — Plateau Spacer System2018-11-26
K160169 — The Life Spine Subtalar Implant System2016-06-23
K150368 — Tarsa-Link Wedge Fixation System2015-03-24
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.