ClearanceBrief
510(k) K230202 · OLO Orthopedic Stereotaxic Instrument

TMINI™ Miniature Robotic System

ApplicantTHINK Surgical, Inc., Fremont CA, US
DecisionSubstantially Equivalent, Apr 25, 2023
ReceivedJan 25, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230202

DateFirm and productCodeLinked 510(k)
Mar 20, 2024Think Surgical, Inc.
Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
Open, Classified
OLONone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.