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FDA 510(k)

CODMAN ARTHROSCOPE

K-Number: K851229 · 1985-05-22

ApplicantCodman & Shurtleff, Inc.
Decision Date1985-05-22
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODMAN ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1985-05-22 under 510(k) number K851229. 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 CODMAN ARTHROSCOPE?

CODMAN ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1985-05-22. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K851229.

When did CODMAN ARTHROSCOPE receive FDA 510(k) clearance?

CODMAN ARTHROSCOPE received FDA 510(k) clearance on 1985-05-22, under 510(k) number K851229.

Who is the listed applicant for CODMAN ARTHROSCOPE?

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

What is the FDA product code for CODMAN ARTHROSCOPE?

The FDA product code for CODMAN ARTHROSCOPE is HRX.

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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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