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FDA 510(k)

CEMENTRALIZER DISTAL STEM CENTRALIZER

K-Number: K951930 · 1995-07-11

ApplicantDepuy, Inc.
Decision Date1995-07-11
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CEMENTRALIZER DISTAL STEM CENTRALIZER is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1995-07-11 under 510(k) number K951930. The device is classified under product code LZN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENTRALIZER DISTAL STEM CENTRALIZER?

CEMENTRALIZER DISTAL STEM CENTRALIZER is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is Depuy, Inc.. The 510(k) number is K951930.

When did CEMENTRALIZER DISTAL STEM CENTRALIZER receive FDA 510(k) clearance?

CEMENTRALIZER DISTAL STEM CENTRALIZER received FDA 510(k) clearance on 1995-07-11, under 510(k) number K951930.

Who is the listed applicant for CEMENTRALIZER DISTAL STEM CENTRALIZER?

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

What is the FDA product code for CEMENTRALIZER DISTAL STEM CENTRALIZER?

The FDA product code for CEMENTRALIZER DISTAL STEM CENTRALIZER is LZN.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: LZN)

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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