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FDA 510(k)

INTERLOK BIO-MODULAR HUMERAL STEMS

K-Number: K032507 · 2003-09-05

ApplicantBiomet, Inc.
Decision Date2003-09-05
Product CodeKWT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERLOK BIO-MODULAR HUMERAL STEMS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2003-09-05 under 510(k) number K032507. The device is classified under product code KWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERLOK BIO-MODULAR HUMERAL STEMS?

INTERLOK BIO-MODULAR HUMERAL STEMS is a medical device that received FDA 510(k) clearance on 2003-09-05. The listed applicant is Biomet, Inc.. The 510(k) number is K032507.

When did INTERLOK BIO-MODULAR HUMERAL STEMS receive FDA 510(k) clearance?

INTERLOK BIO-MODULAR HUMERAL STEMS received FDA 510(k) clearance on 2003-09-05, under 510(k) number K032507.

Who is the listed applicant for INTERLOK BIO-MODULAR HUMERAL STEMS?

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

What is the FDA product code for INTERLOK BIO-MODULAR HUMERAL STEMS?

The FDA product code for INTERLOK BIO-MODULAR HUMERAL STEMS is KWT.

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Related Devices (Code: KWT)

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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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