Cementralizer Distal Stem Centralizer

FDA 510(k) K951930 · Depuy, Inc.

Substantially Equivalent

510(k) numberK951930

Submission

Device name
Cementralizer Distal Stem Centralizer
Applicant
Depuy, Inc.
Warsaw, IN, US
Received
April 5, 1995
Decision date
July 11, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LZN – Cement Obturator
Device class
Class II (moderate risk)
Regulation
21 CFR 878.3300
Specialty
General, Plastic Surgery
Implant
Yes

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K061824Tornier Cement RestrictorLZN · Traditional Tornier09/14/2006SE
K032685Cemstop Cement RestrictorLZN · Traditional Teknimed, S.A.11/26/2003SE
K023680Biobuck Cement RestrictorLZN · Special Smith & Nephew, Inc.11/19/2002SE
K011943Impro Vise Absorbable Cement Flow RestrictorLZN · Traditional Kensey Nash Corp.09/19/2001SE
K010840SynplugLZN · Special Isotis NV04/20/2001SE
K993841Cemstop Cement RestrictorLZN · Traditional Encore Orthopedics, Inc.05/04/2000SE
K000587Shuttle StopLZN · Traditional Isotis NV05/04/2000SE
K992462Osteonics Universal Distal Cement PlugLZN · Traditional Howmedica Osteonics Corp.08/13/1999SE
K972411Link Cement PlugLZN · Traditional Turnkey Intergration USA, Inc.08/29/1997SE

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Questions and answers

When was Cementralizer Distal Stem Centralizer cleared by the FDA?

Cementralizer Distal Stem Centralizer (K951930) received a 510(k) decision of Substantially Equivalent on July 11, 1995, 97 days after the submission was received.

What is the product code of K951930?

The FDA product code is LZN – Cement Obturator, a Class II (moderate risk) device regulated under 21 CFR 878.3300.