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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