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FDA 510(k) Applications Submitted by JD Webb
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100544
02/25/2010
IMPIX LUMBAR INTERBODY DEVICE
MEDICREA TECHNOLOGIES
K150772
03/24/2015
Snap-Off Self-Compressive Screw
NEOSTEO
K131471
05/22/2013
SELF-COMPRESSIVE SCREW
NEOSTEO
K212545
08/12/2021
FlexitSystem Knee osteotomy system
Neosteo
K072922
10/15/2007
3S HEMI TOE
TRILLIANT SURGICAL LTD
K153182
11/03/2015
SELF- COMPRESSIVE SCREW
NEOSTEO
K043174
11/16/2004
STEALTH FUSION SYSTEM, MODEL RR 1000
R&R MEDICAL, INC.
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