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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Sacroiliac Joint Fixation
510(k) Number K240720
Device Name TiLink-P SI Joint Fusion System
Applicant
SurGenTec, LLC
911 Clint Moore Rd
Boca Raton,  FL  33487
Applicant Contact Guilherme Pires
Correspondent
SurGenTec, LLC
911 Clint Moore Rd
Boca Raton,  FL  33487
Correspondent Contact Guilherme Pires
Regulation Number888.3040
Classification Product Code
OUR  
Date Received03/15/2024
Decision Date 04/11/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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