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FDA 510(k)

MARTIN-CHAMPY TITAN SET

K-Number: K884523 · 1988-12-08

ApplicantBuschmann Surgical Products
Decision Date1988-12-08
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MARTIN-CHAMPY TITAN SET is the device name listed in this FDA 510(k) record. The listed applicant is Buschmann Surgical Products. It received FDA 510(k) clearance on 1988-12-08 under 510(k) number K884523. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN-CHAMPY TITAN SET?

MARTIN-CHAMPY TITAN SET is a medical device that received FDA 510(k) clearance on 1988-12-08. The listed applicant is Buschmann Surgical Products. The 510(k) number is K884523.

When did MARTIN-CHAMPY TITAN SET receive FDA 510(k) clearance?

MARTIN-CHAMPY TITAN SET received FDA 510(k) clearance on 1988-12-08, under 510(k) number K884523.

Who is the listed applicant for MARTIN-CHAMPY TITAN SET?

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

What is the FDA product code for MARTIN-CHAMPY TITAN SET?

The FDA product code for MARTIN-CHAMPY TITAN SET is JEY.

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Related Devices (Code: JEY)

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

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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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