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FDA 510(k) Applications Submitted by LINVATEC CORPORATION D/B/A CONMED LINVATEC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112965
10/05/2011
NANO SUTURE ANCHOR
LINVATEC CORPORATION D/B/A CONMED LINVATEC
K130497
02/26/2013
D4000 DRIVE SYSTEM; D4000A DRIVE SYSTEM WITH IRRIGATION
LINVATEC CORPORATION D/B/A CONMED LINVATEC
K131035
04/12/2013
Y-KNOT FLEX ALL-SUTURE ANCHOR, W/ TWO #2 (5 METRIC) HI-FI SUTURES, 1.8MM
LINVATEC CORPORATION D/B/A CONMED LINVATEC
K121890
06/28/2012
GENESYS PRESSFT SUTURE ANCHOR
LINVATEC CORPORATION D/B/A CONMED LINVATEC
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