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FDA 510(k)

EUCLID REDUCTION AND GUIDANCE SYSTEM

K-Number: K991037 · 1999-06-23

ApplicantModular Cutting Systems, Inc.
Decision Date1999-06-23
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EUCLID REDUCTION AND GUIDANCE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Modular Cutting Systems, Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991037. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUCLID REDUCTION AND GUIDANCE SYSTEM?

EUCLID REDUCTION AND GUIDANCE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Modular Cutting Systems, Inc.. The 510(k) number is K991037.

When did EUCLID REDUCTION AND GUIDANCE SYSTEM receive FDA 510(k) clearance?

EUCLID REDUCTION AND GUIDANCE SYSTEM received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991037.

Who is the listed applicant for EUCLID REDUCTION AND GUIDANCE SYSTEM?

The FDA 510(k) record lists Modular Cutting Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUCLID REDUCTION AND GUIDANCE SYSTEM?

The FDA product code for EUCLID REDUCTION AND GUIDANCE SYSTEM is JDS.

Related Clinical Trials

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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Other records listing Modular Cutting Systems, Inc. as applicant

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.

K990816AVCORE SYSTEM

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Official Source

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