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510(k) Predicate Database
FDA 510(k) ClearanceHRS

APTUS Clavicle System 2.8

FDA 510(k) K260761 · Medartis AG

510(k) number
K260761
Device name
APTUS Clavicle System 2.8
Applicant
Medartis AG
Product code
HRS
Decision
Substantially Equivalent
Decision date
2026-06-05
Device class
Class 2
Regulation number
888.3030
Advisory committee
Orthopedic
Medical specialty
Orthopedic

Candidate predicate devices

Other devices cleared under product code HRS — the same regulatory device type, and therefore candidate predicates for a substantial-equivalence comparison. Confirm each predicate is legally marketed before relying on it.

510(k)DeviceApplicantDecision date
K261002Pectus Blu SystemBiomet Microfixation2026-06-02
K261038Xpert PFPNewclip Technics2026-05-29
K261145Avanti Distal Elbow ORIF SystemAvanti Orthopaedics, LLC2026-05-09
K260323OrthoPediatrics® Locking Cannulated Blade Plate SystemOrthoPediatrics Corp.2026-04-30
K260228POYA 3.5mm Medial Proximal Tibia SystemBonebridge AG2026-04-24
K260411PC Fix SystemChest Wall Innovations, Inc.2026-04-24
K260054I.T.S. PRS Phoenix III.T.S. GmbH2026-04-24
K260090SMART Osteotomy SystemActis Medical Pty., Ltd.2026-04-10
K253718enHAnce PEEK Bunion SystemNvision Biomedical Technologies, Inc.2026-04-01
K260274Airlock® Ankle Plating SystemNovastep SAS2026-03-25
K260291Vortex5 Tailor's Bunion Correction SystemNvision Biomedical Technologies, Inc.2026-03-25

Building a 510(k) around this device type?

Assyro turns predicate research into a substantial-equivalence comparison and an eSTAR-ready 510(k) workflow — so predicate strategy, testing evidence, and labeling stay aligned before FDA review.