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FDA 510(k)

THACKRAY TOTAL CONDYLAR KNEES

K-Number: K855166 · 1986-03-13

ApplicantThackray USA
Decision Date1986-03-13
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THACKRAY TOTAL CONDYLAR KNEES is the device name listed in this FDA 510(k) record. The listed applicant is Thackray USA. It received FDA 510(k) clearance on 1986-03-13 under 510(k) number K855166. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THACKRAY TOTAL CONDYLAR KNEES?

THACKRAY TOTAL CONDYLAR KNEES is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Thackray USA. The 510(k) number is K855166.

When did THACKRAY TOTAL CONDYLAR KNEES receive FDA 510(k) clearance?

THACKRAY TOTAL CONDYLAR KNEES received FDA 510(k) clearance on 1986-03-13, under 510(k) number K855166.

Who is the listed applicant for THACKRAY TOTAL CONDYLAR KNEES?

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

What is the FDA product code for THACKRAY TOTAL CONDYLAR KNEES?

The FDA product code for THACKRAY TOTAL CONDYLAR KNEES is JWH.

Related Clinical Trials

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.

Other records listing Thackray USA 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.

Related Devices (Code: JWH)

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.

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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