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FDA 510(k) Applications Submitted by ICOTEC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100305
02/03/2010
ETURN SPINAL IMPLANT MODEL ETURN XX-12; ETURN XX-16 WHERE XX=07, 09, 11, 13, OR 15 AND ETURN XX-12 K; ETURN XX-16 K WHER
ICOTEC
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