SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310) by ABBOTT SPINE, INC. | FDA 510(k) Summary

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K Number

Validate with FDA (Live)

Device Name

SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310)

Manufacturer

ABBOTT SPINE, INC.

Date Cleared

2008-10-06

(81 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K100845,K101682,K111301,K113270,K122592,K123552,K131980,K132884

Intended Use

Device Description

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Regulation Number and Section

N/A