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FDA 510(k)

SEIDEL INTRAMEDULLARY PLUG

K-Number: K792205 · 1979-12-06

ApplicantHowmedica Corp.
Decision Date1979-12-06
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEIDEL INTRAMEDULLARY PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792205. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEIDEL INTRAMEDULLARY PLUG?

SEIDEL INTRAMEDULLARY PLUG is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Howmedica Corp.. The 510(k) number is K792205.

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

SEIDEL INTRAMEDULLARY PLUG received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792205.

Who is the listed applicant for SEIDEL INTRAMEDULLARY PLUG?

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

What is the FDA product code for SEIDEL INTRAMEDULLARY PLUG?

The FDA product code for SEIDEL INTRAMEDULLARY PLUG is HWC. This falls under the Cardiovascular category.

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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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