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FDA 510(k)

LEFORTE SYSTEM BONE PLATE

K-Number: K023360 · 2002-10-25

ApplicantJeil Medical Corporation
Decision Date2002-10-25
Product CodeKTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LEFORTE SYSTEM BONE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Jeil Medical Corporation. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K023360. The device is classified under product code KTW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEFORTE SYSTEM BONE PLATE?

LEFORTE SYSTEM BONE PLATE is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Jeil Medical Corporation. The 510(k) number is K023360.

When did LEFORTE SYSTEM BONE PLATE receive FDA 510(k) clearance?

LEFORTE SYSTEM BONE PLATE received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023360.

Who is the listed applicant for LEFORTE SYSTEM BONE PLATE?

The FDA 510(k) record lists Jeil Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEFORTE SYSTEM BONE PLATE?

The FDA product code for LEFORTE SYSTEM BONE PLATE is KTW.

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Related Devices (Code: KTW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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