FDA 510(k)

BARD INTRAMEDULLARY PLUG

K-Number: K831128 · 1983-07-12

Decision Date1983-07-12

Product CodeJDK

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BARD INTRAMEDULLARY PLUG is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831128. The device is classified under product code JDK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD INTRAMEDULLARY PLUG?

BARD INTRAMEDULLARY PLUG is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K831128.

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

BARD INTRAMEDULLARY PLUG received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831128.

Who is the listed applicant for BARD INTRAMEDULLARY PLUG?

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

What is the FDA product code for BARD INTRAMEDULLARY PLUG?

The FDA product code for BARD INTRAMEDULLARY PLUG is JDK.

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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.