Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ADG BONE PLUG

K-Number: K902615 · 1990-09-11

ApplicantAmerican Design Group, Inc.
Decision Date1990-09-11
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADG BONE PLUG 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 1990-09-11 under 510(k) number K902615. 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 BONE PLUG?

ADG BONE PLUG is a medical device that received FDA 510(k) clearance on 1990-09-11. The listed applicant is American Design Group, Inc.. The 510(k) number is K902615.

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

ADG BONE PLUG received FDA 510(k) clearance on 1990-09-11, under 510(k) number K902615.

Who is the listed applicant for ADG BONE PLUG?

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 BONE PLUG?

The FDA product code for ADG BONE PLUG is LZN.

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.

K911717ADG INTRAMEDULLARY BONE PLUG - VENTEDK890722ADG 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑