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Parker Quality & Compliance

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510(k) clearance

Odys-SI Screw

FDA 510(k) source

510(k) number
K262522
Applicant
Medyssey Co, Ltd.
Decision date
Oct 15, 2026
Date received
Jul 22, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
OUR
Device type
Sacroiliac Joint Fixation
Device class
Class II
Regulation
21 CFR 888.3040
Advisory committee
Orthopedic
Statement or summary
Summary
Third party
N
Location
Jecheon-Si, KR