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FDA 510(k)

CORIN MODULAR MOORE STEM

K-Number: K881288 · 1988-06-29

Decision Date1988-06-29
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN MODULAR MOORE STEM is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1988-06-29 under 510(k) number K881288. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORIN MODULAR MOORE STEM?

CORIN MODULAR MOORE STEM is a medical device that received FDA 510(k) clearance on 1988-06-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K881288.

When did CORIN MODULAR MOORE STEM receive FDA 510(k) clearance?

CORIN MODULAR MOORE STEM received FDA 510(k) clearance on 1988-06-29, under 510(k) number K881288.

Who is the listed applicant for CORIN MODULAR MOORE STEM?

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

What is the FDA product code for CORIN MODULAR MOORE STEM?

The FDA product code for CORIN MODULAR MOORE STEM is LWJ.

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.

Other records listing Orthopedic 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.

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Related Devices (Code: LWJ)

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.

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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