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FDA 510(k)

RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS

K-Number: K893377 · 1989-11-16

ApplicantRichards Medical Co., Inc.
Decision Date1989-11-16
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1989-11-16 under 510(k) number K893377. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS?

RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS is a medical device that received FDA 510(k) clearance on 1989-11-16. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K893377.

When did RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS receive FDA 510(k) clearance?

RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS received FDA 510(k) clearance on 1989-11-16, under 510(k) number K893377.

Who is the listed applicant for RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS?

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

What is the FDA product code for RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS?

The FDA product code for RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS is HSB.

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Other records listing Richards Medical Co., Inc. as applicant

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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