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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

MODIFICATION TO SYNERGY SPINAL SYSTEM

Manufacturer

INTERPORE CROSS INTL.

Date Cleared

2001-03-22

(28 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K020085,K070966,K072426,K232341

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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AI/ML Overview

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