SPINAL SPHERES— 510(k) K062992

Unknown

Interbody Innovations, Llp

FDA 510(k) clearance K062992 for SPINAL SPHERES, Unknown on 2007-07-27. Applicant: Interbody Innovations, Llp. Device class: 3.

Clearance details

Applicant: Interbody Innovations, Llp
Product code: Code NVR
Device class: Class 3
Advisory panel: Unknown
Date received: 2006-10-02
Decision date: 2007-07-27
Decision: Unknown
Clearance type: Traditional
Location: Round Rock, TX, US

Download summary PDF View on FDA.gov ↗

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K060415 — MODIFICATION TO: SATELLITE SPINAL SYSTEM2007-01-05
K051320 — SATELLITE SPINAL SYSTEM2005-09-09

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