Sintea Plustek, LLC

Sintea Plustek, LLC holds 3 FDA 510(k) medical device clearances, first cleared 2012, most recent 2014.

Top product codes for Sintea Plustek, LLC

Recent clearances by Sintea Plustek, LLC

K140787 — PLS (POSTERIOR LUMBAR SYSTEM)Code MNH·2014-05-30
K130402 — SPIDER SYSTEM KOLIBRI CEMENT NEEDLECode NDN·2013-04-01
K112861 — SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEMCode KWQ·2012-02-24

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