FDA 510(k)

LEIBINGER NEURO CLIP SYSTEM

K-Number: K003660 · 2000-12-12

Decision Date2000-12-12

Product CodeJEY

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

LEIBINGER NEURO CLIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2000-12-12 under 510(k) number K003660. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEIBINGER NEURO CLIP SYSTEM?

LEIBINGER NEURO CLIP SYSTEM is a medical device that received FDA 510(k) clearance on 2000-12-12. The listed applicant is Stryker Instruments. The 510(k) number is K003660.

When did LEIBINGER NEURO CLIP SYSTEM receive FDA 510(k) clearance?

LEIBINGER NEURO CLIP SYSTEM received FDA 510(k) clearance on 2000-12-12, under 510(k) number K003660.

Who is the listed applicant for LEIBINGER NEURO CLIP SYSTEM?

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

What is the FDA product code for LEIBINGER NEURO CLIP SYSTEM?

The FDA product code for LEIBINGER NEURO CLIP SYSTEM is JEY.

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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.