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FDA 510(k) Applications Submitted by Martin Ostmann
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122139
07/19/2012
SMITH & NEPHEW R3 CONSTRAINED LINERS
SMITH & NEPHEW, INC.
K132296
07/23/2013
D-RAD SMART PACK
SMITH & NEPHEW, INC.
K142520
09/08/2014
Smith & Nephew, Inc. Spatialframe.com V5.0 Web-based software
Smith & Nephew, Inc
K123159
10/09/2012
SMITH & NEWPHEW, INC. DISPOSABLE KNEE INSTRUMENTS
SMITH & NEPHEW, INC.
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