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FDA 510(k)

FEMORAL HOOK

K-Number: K041261 · 2004-06-07

ApplicantArthrotek, Inc.
Decision Date2004-06-07
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FEMORAL HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Arthrotek, Inc.. It received FDA 510(k) clearance on 2004-06-07 under 510(k) number K041261. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL HOOK?

FEMORAL HOOK is a medical device that received FDA 510(k) clearance on 2004-06-07. The listed applicant is Arthrotek, Inc.. The 510(k) number is K041261.

When did FEMORAL HOOK receive FDA 510(k) clearance?

FEMORAL HOOK received FDA 510(k) clearance on 2004-06-07, under 510(k) number K041261.

Who is the listed applicant for FEMORAL HOOK?

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

What is the FDA product code for FEMORAL HOOK?

The FDA product code for FEMORAL HOOK is MBI.

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Other records listing Arthrotek, 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: MBI)

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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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