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FDA 510(k)

CENTERING PLUG

K-Number: K900392 · 1990-03-01

ApplicantAllo Pro Corp.
Decision Date1990-03-01
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CENTERING PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1990-03-01 under 510(k) number K900392. 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 CENTERING PLUG?

CENTERING PLUG is a medical device that received FDA 510(k) clearance on 1990-03-01. The listed applicant is Allo Pro Corp.. The 510(k) number is K900392.

When did CENTERING PLUG receive FDA 510(k) clearance?

CENTERING PLUG received FDA 510(k) clearance on 1990-03-01, under 510(k) number K900392.

Who is the listed applicant for CENTERING PLUG?

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

What is the FDA product code for CENTERING PLUG?

The FDA product code for CENTERING PLUG is LZN.

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Other records listing Allo Pro Corp. 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.

K901581GSB ELBOWK900425SURGICAL COTTON GLOVESK896669WEBER PERMALOCKK892644BIOLOX CERAMIC BALLK885049RS-CUP ACETABULAR PROSTHESISK864999KENNEDY STEM

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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.

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