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FDA 510(k)

CENATOR TOTAL HIP SYSTEM

K-Number: K925866 · 1993-09-23

Decision Date1993-09-23
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CENATOR TOTAL HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Corin Orthopedic Products. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K925866. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENATOR TOTAL HIP SYSTEM?

CENATOR TOTAL HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Corin Orthopedic Products. The 510(k) number is K925866.

When did CENATOR TOTAL HIP SYSTEM receive FDA 510(k) clearance?

CENATOR TOTAL HIP SYSTEM received FDA 510(k) clearance on 1993-09-23, under 510(k) number K925866.

Who is the listed applicant for CENATOR TOTAL HIP SYSTEM?

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

What is the FDA product code for CENATOR TOTAL HIP SYSTEM?

The FDA product code for CENATOR TOTAL HIP SYSTEM is JDI.

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 Corin Orthopedic Products 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: JDI)

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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