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FDA 510(k)

POLYETHYLENE MEDULLARY PLUG - STIIHMER/

K-Number: K830949 · 1983-04-12

ApplicantAllo Pro Corp.
Decision Date1983-04-12
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POLYETHYLENE MEDULLARY PLUG - STIIHMER/ 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 1983-04-12 under 510(k) number K830949. 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 POLYETHYLENE MEDULLARY PLUG - STIIHMER/?

POLYETHYLENE MEDULLARY PLUG - STIIHMER/ is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Allo Pro Corp.. The 510(k) number is K830949.

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

POLYETHYLENE MEDULLARY PLUG - STIIHMER/ received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830949.

Who is the listed applicant for POLYETHYLENE MEDULLARY PLUG - STIIHMER/?

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 POLYETHYLENE MEDULLARY PLUG - STIIHMER/?

The FDA product code for POLYETHYLENE MEDULLARY PLUG - STIIHMER/ is LZN.

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Other records listing Allo Pro Corp. as applicant

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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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