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FDA 510(k) Applications Submitted by MELISSA EGAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112526
08/31/2011
TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS
SMITH & NEPHEW, INC.
K113274
11/07/2011
FOOTPRINT ULTRA PK SUTURE ANCHOR
SMITH & NEPHEW, INC.
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