CEMSTOP CEMENT RESTRICTOR— 510(k) K032685

Substantially Equivalent

Teknimed, S.A.

FDA 510(k) clearance K032685 for CEMSTOP CEMENT RESTRICTOR, Substantially Equivalent on 2003-11-26. Applicant: Teknimed, S.A.. Device class: 2.

Clearance details

Applicant: Teknimed, S.A.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-08-29
Decision date: 2003-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Rock, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZN

K220838 — Artisan Bone Plug, Universal Cement Restrictor2022-05-20
K061824 — TORNIER CEMENT RESTRICTOR2006-09-14
K023680 — BIOBUCK CEMENT RESTRICTOR2002-11-19
K011943 — IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR2001-09-19
K010840 — SYNPLUG2001-04-20

More clearances from Teknimed, S.A.

K103433 — F202011-01-03
K090435 — VERTECEM2009-12-21
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K080873 — OPACITY + BONE CEMENT2008-08-28
K062102 — ODONCER2007-04-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.