PLS (POSTERIOR LUMBAR SYSTEM)

• K Number: K140787
• Device Name: PLS (POSTERIOR LUMBAR SYSTEM)
• Manufacturer: SINTEA PLUSTEK, LLC
• Date Cleared: 2014-05-30 ( 60 days)
• Product Code: MNH , KWP , MNI
• Regulation Number: 888.3070
• Type: Special
• Panel: Orthopedic
• Reference & Predicate Devices: N/A
• Predicate For: N/A

Intended Use

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Device Description

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AI/ML Overview

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Summary

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Regulation Number and Section

N/A