LORENZ STERNAL CLOSURE SYSTEM WITH MODULAR SCREW by WALTER LORENZ SURGICAL, INC. | FDA 510(k) Summary

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K Number

Validate with FDA (Live)

Device Name

LORENZ STERNAL CLOSURE SYSTEM WITH MODULAR SCREW

Manufacturer

WALTER LORENZ SURGICAL, INC.

Date Cleared

2001-07-16

(98 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K033740,K053624,K063506,K101170,K110039,K110574,K111908,K121302,K122293

Intended Use

Device Description

AI/ML Overview

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Regulation Number and Section

N/A