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FDA 510(k)

ORTHOPAEDIC POLYETHYLENE CABLE

K-Number: K924141 · 1993-11-30

ApplicantSmith & Nephew Richards, Inc.
Decision Date1993-11-30
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOPAEDIC POLYETHYLENE CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1993-11-30 under 510(k) number K924141. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPAEDIC POLYETHYLENE CABLE?

ORTHOPAEDIC POLYETHYLENE CABLE is a medical device that received FDA 510(k) clearance on 1993-11-30. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K924141.

When did ORTHOPAEDIC POLYETHYLENE CABLE receive FDA 510(k) clearance?

ORTHOPAEDIC POLYETHYLENE CABLE received FDA 510(k) clearance on 1993-11-30, under 510(k) number K924141.

Who is the listed applicant for ORTHOPAEDIC POLYETHYLENE CABLE?

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

What is the FDA product code for ORTHOPAEDIC POLYETHYLENE CABLE?

The FDA product code for ORTHOPAEDIC POLYETHYLENE CABLE is JDQ.

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Other records listing Smith & Nephew Richards, Inc. as applicant

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Related Devices (Code: JDQ)

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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