FDA 510(k) Applications Submitted by NEOSTEO

FDA 510(k) Number Submission Date Device Name Applicant
K191424 05/29/2019 Interphalangeal Joint Fusion Device Range Neosteo
K192447 09/06/2019 Superelastic Staple Neosteo
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
K153182 11/03/2015 SELF- COMPRESSIVE SCREW NEOSTEO


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