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FDA 510(k)

EXETER INTRAMEDULLARY BONE PLUG

K-Number: K980843 · 1998-06-02

ApplicantHowmedica, Inc.
Decision Date1998-06-02
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXETER INTRAMEDULLARY BONE PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Inc.. It received FDA 510(k) clearance on 1998-06-02 under 510(k) number K980843. 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 EXETER INTRAMEDULLARY BONE PLUG?

EXETER INTRAMEDULLARY BONE PLUG is a medical device that received FDA 510(k) clearance on 1998-06-02. The listed applicant is Howmedica, Inc.. The 510(k) number is K980843.

When did EXETER INTRAMEDULLARY BONE PLUG receive FDA 510(k) clearance?

EXETER INTRAMEDULLARY BONE PLUG received FDA 510(k) clearance on 1998-06-02, under 510(k) number K980843.

Who is the listed applicant for EXETER INTRAMEDULLARY BONE PLUG?

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

What is the FDA product code for EXETER INTRAMEDULLARY BONE PLUG?

The FDA product code for EXETER INTRAMEDULLARY BONE PLUG is JDI.

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Other records listing Howmedica, Inc. as applicant

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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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