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FDA 510(k)

ARTHROCOMBI 5003

K-Number: K871181 · 1987-09-29

ApplicantF.M. Wiest USA, Inc.
Decision Date1987-09-29
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROCOMBI 5003 is the device name listed in this FDA 510(k) record. The listed applicant is F.M. Wiest USA, Inc.. It received FDA 510(k) clearance on 1987-09-29 under 510(k) number K871181. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROCOMBI 5003?

ARTHROCOMBI 5003 is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is F.M. Wiest USA, Inc.. The 510(k) number is K871181.

When did ARTHROCOMBI 5003 receive FDA 510(k) clearance?

ARTHROCOMBI 5003 received FDA 510(k) clearance on 1987-09-29, under 510(k) number K871181.

Who is the listed applicant for ARTHROCOMBI 5003?

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

What is the FDA product code for ARTHROCOMBI 5003?

The FDA product code for ARTHROCOMBI 5003 is HRX.

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Other records listing F.M. Wiest USA, Inc. as applicant

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Related Devices (Code: HRX)

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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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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