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FDA 510(k)

LESTER PRESS FIT HIP PROSTHESIS

K-Number: K915500 · 1992-10-20

ApplicantKirschner Medical Corp.
Decision Date1992-10-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LESTER PRESS FIT HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K915500. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LESTER PRESS FIT HIP PROSTHESIS?

LESTER PRESS FIT HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K915500.

When did LESTER PRESS FIT HIP PROSTHESIS receive FDA 510(k) clearance?

LESTER PRESS FIT HIP PROSTHESIS received FDA 510(k) clearance on 1992-10-20, under 510(k) number K915500.

Who is the listed applicant for LESTER PRESS FIT HIP PROSTHESIS?

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

What is the FDA product code for LESTER PRESS FIT HIP PROSTHESIS?

The FDA product code for LESTER PRESS FIT HIP PROSTHESIS is JDI.

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Other records listing Kirschner Medical Corp. as applicant

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Related Devices (Code: JDI)

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Official Source

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

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