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FDA 510(k) Applications Submitted by CAROL EMERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090767
03/23/2009
PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
INTERVENTIONAL SPINE, INC.
K082795
09/23/2008
SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT
INTERVENTIONAL SPINE, INC.
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