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FDA 510(k)

POLYETHYLENE MEDULLARY PLUG

K-Number: K811060 · 1981-05-01

ApplicantArthur A. Checchi, Inc.
Decision Date1981-05-01
Product Code
DecisionSubstantially Equivalent

Device Summary

POLYETHYLENE MEDULLARY PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Arthur A. Checchi, Inc.. It received FDA 510(k) clearance on 1981-05-01 under 510(k) number K811060. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYETHYLENE MEDULLARY PLUG?

POLYETHYLENE MEDULLARY PLUG is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Arthur A. Checchi, Inc.. The 510(k) number is K811060.

When did POLYETHYLENE MEDULLARY PLUG receive FDA 510(k) clearance?

POLYETHYLENE MEDULLARY PLUG received FDA 510(k) clearance on 1981-05-01, under 510(k) number K811060.

Who is the listed applicant for POLYETHYLENE MEDULLARY PLUG?

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

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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