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FDA 510(k) Applications Submitted by KATI MARTTINEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090177
01/23/2009
INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE
INION OY
K070998
04/09/2007
INION BIORESTORE
INION OY
K151360
05/20/2015
Inion Spinal Graft Containment System
Inion Oy
K071464
05/29/2007
INION HEXALON BIODEGRADABLE ACL/PCL SCREW
INION OY
K071810
07/02/2007
INION SPINAL GRAFT CONTAINMENT SYSTEM
INION LTD.
K062782
09/18/2006
INION ANCHRON PLUS BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-6001
INION OY
K122890
09/20/2012
INION CPS ORBITAL PLATES
INION OY
K203105
10/15/2020
Inion CompressOn Screw
Inion Oy
K063410
11/13/2006
INION CPS/OTPS FREEDOMPLATE
INION LTD.
K123672
11/29/2012
INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FREEDOMSCREW)
INION OY
K133932
12/23/2013
INION FREEDOMPIN
INION OY
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