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FDA 510(k)

NEXUS ACETABULAR CUP

K-Number: K905408 · 1991-03-01

ApplicantDow Corning Wright
Decision Date1991-03-01
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEXUS ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1991-03-01 under 510(k) number K905408. 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 NEXUS ACETABULAR CUP?

NEXUS ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1991-03-01. The listed applicant is Dow Corning Wright. The 510(k) number is K905408.

When did NEXUS ACETABULAR CUP receive FDA 510(k) clearance?

NEXUS ACETABULAR CUP received FDA 510(k) clearance on 1991-03-01, under 510(k) number K905408.

Who is the listed applicant for NEXUS ACETABULAR CUP?

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

What is the FDA product code for NEXUS ACETABULAR CUP?

The FDA product code for NEXUS ACETABULAR CUP is JDI.

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Other records listing Dow Corning Wright 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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Related Devices (Code: JDI)

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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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