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FDA 510(k) Applications Submitted by MIKE ROSENTHAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161191
04/27/2016
Latera Absorbable Nasal Implant
SPIROX, INC.
K132920
09/17/2013
SPIROX INEX DEVICE
SPIROX, INC.
K142643
09/17/2014
Stabilynx PEEK Suture Anchor
D3 DC, LLC /Stabilynx, Inc
K152958
10/07/2015
INEX Absorbable Nasal Implant
SPIROX, INC.
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