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FDA 510(k)

ARTHRODISTRACTOR

K-Number: K896770 · 1990-01-02

ApplicantArthroplastics, Inc.
Decision Date1990-01-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHRODISTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Arthroplastics, Inc.. It received FDA 510(k) clearance on 1990-01-02 under 510(k) number K896770. 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 ARTHRODISTRACTOR?

ARTHRODISTRACTOR is a medical device that received FDA 510(k) clearance on 1990-01-02. The listed applicant is Arthroplastics, Inc.. The 510(k) number is K896770.

When did ARTHRODISTRACTOR receive FDA 510(k) clearance?

ARTHRODISTRACTOR received FDA 510(k) clearance on 1990-01-02, under 510(k) number K896770.

Who is the listed applicant for ARTHRODISTRACTOR?

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

What is the FDA product code for ARTHRODISTRACTOR?

The FDA product code for ARTHRODISTRACTOR is HRX.

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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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