ClearanceBrief
510(k) K051567 ยท HRS Plate, Fixation, Bone

APTUS TITANIUM OSTEOSYNTHESIS SYSTEM

ApplicantMedartis, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Aug 23, 2005
ReceivedJun 14, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051567

DateFirm and productCodeLinked 510(k)
Mar 10, 2026Medartis AG
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for frac
Open, Classified
HWCNone listed

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