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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 K231831
Device Name TiLink-L Joint Fusion System
Applicant
Surgentec
911 Clint Moore Rd.
Boca Raton,  FL  33487
Applicant Contact Andrew Shoup
Correspondent
Surgentec
911 Clint Moore Rd.
Boca Raton,  FL  33487
Correspondent Contact Andrew Shoup
Regulation Number888.3040
Classification Product Code
OUR  
Date Received06/22/2023
Decision Date 08/03/2023
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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