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FDA 510(k)

ARTHRO-SURGIMAT-A103

K-Number: K000153 · 2000-02-08

ApplicantW.O.M. World of Medicine GmbH
Decision Date2000-02-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHRO-SURGIMAT-A103 is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 2000-02-08 under 510(k) number K000153. 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 ARTHRO-SURGIMAT-A103?

ARTHRO-SURGIMAT-A103 is a medical device that received FDA 510(k) clearance on 2000-02-08. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K000153.

When did ARTHRO-SURGIMAT-A103 receive FDA 510(k) clearance?

ARTHRO-SURGIMAT-A103 received FDA 510(k) clearance on 2000-02-08, under 510(k) number K000153.

Who is the listed applicant for ARTHRO-SURGIMAT-A103?

The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHRO-SURGIMAT-A103?

The FDA product code for ARTHRO-SURGIMAT-A103 is HRX.

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Related Devices (Code: HRX)

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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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