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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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