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FDA 510(k)

INTRAMEDULLARY BONE PLUG

K-Number: K832328 · 1983-10-20

ApplicantKirschner Medical Corp.
Decision Date1983-10-20
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTRAMEDULLARY BONE PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1983-10-20 under 510(k) number K832328. 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 INTRAMEDULLARY BONE PLUG?

INTRAMEDULLARY BONE PLUG is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K832328.

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

INTRAMEDULLARY BONE PLUG received FDA 510(k) clearance on 1983-10-20, under 510(k) number K832328.

Who is the listed applicant for INTRAMEDULLARY BONE PLUG?

The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRAMEDULLARY BONE PLUG?

The FDA product code for INTRAMEDULLARY BONE PLUG is JDS.

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Other records listing Kirschner Medical Corp. as applicant

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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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