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FDA 510(k)

ADG INTRAMEDULLARY BONE PLUG - VENTED

K-Number: K911717 · 1991-09-04

ApplicantAmerican Design Group, Inc.
Decision Date1991-09-04
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADG INTRAMEDULLARY BONE PLUG - VENTED is the device name listed in this FDA 510(k) record. The listed applicant is American Design Group, Inc.. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K911717. The device is classified under product code LZN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADG INTRAMEDULLARY BONE PLUG - VENTED?

ADG INTRAMEDULLARY BONE PLUG - VENTED is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is American Design Group, Inc.. The 510(k) number is K911717.

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

ADG INTRAMEDULLARY BONE PLUG - VENTED received FDA 510(k) clearance on 1991-09-04, under 510(k) number K911717.

Who is the listed applicant for ADG INTRAMEDULLARY BONE PLUG - VENTED?

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

What is the FDA product code for ADG INTRAMEDULLARY BONE PLUG - VENTED?

The FDA product code for ADG INTRAMEDULLARY BONE PLUG - VENTED is LZN.

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Other records listing American Design Group, Inc. as applicant

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.

K902615ADG BONE PLUGK890722ADG BONE BIOPSY SYSTEM

Related Devices (Code: LZN)

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.

K220838Artisan Bone Plug, Universal Cement RestrictorHowmedica Osteonics, Dba Stryker OrthopaedicsK061824TORNIER CEMENT RESTRICTORTornierK032685CEMSTOP CEMENT RESTRICTORTeknimed, S.A.K023680BIOBUCK CEMENT RESTRICTORSmith & Nephew, Inc.K011943IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTORKensey Nash Corp.K010840SYNPLUGIsotis NV

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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