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FDA 510(k)

FUSON BONE PLUG, RADIOPAQUE

K-Number: K800142 · 1980-02-19

ApplicantZimmer, Inc.
Decision Date1980-02-19
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FUSON BONE PLUG, RADIOPAQUE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K800142. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUSON BONE PLUG, RADIOPAQUE?

FUSON BONE PLUG, RADIOPAQUE is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Zimmer, Inc.. The 510(k) number is K800142.

When did FUSON BONE PLUG, RADIOPAQUE receive FDA 510(k) clearance?

FUSON BONE PLUG, RADIOPAQUE received FDA 510(k) clearance on 1980-02-19, under 510(k) number K800142.

Who is the listed applicant for FUSON BONE PLUG, RADIOPAQUE?

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

What is the FDA product code for FUSON BONE PLUG, RADIOPAQUE?

The FDA product code for FUSON BONE PLUG, RADIOPAQUE is JDS.

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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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