Avitus Orthopaedics, Inc.
Avitus Orthopaedics, Inc. holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2023, with 2 FDA device recalls on record.
Top product codes for Avitus Orthopaedics, Inc.
FDA recalls by Avitus Orthopaedics, Inc.
- Z-1047-2019 — Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow
- Z-1046-2019 — Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-110 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Avitus Orthopaedics, Inc.
- K231456 — Avitus® DragonWing Large Volume Autograft Delivery System
- K230492 — Avitus® Precision Autograft Delivery System
- K210631 — Avitus(r) Bone Harvester
- K170539 — Avitus Bone Harvester with Filter Insert - 5mm, Avitus Bone Harvester - 5mm, Avitus Bone Harvester with Filter Insert - 8mm, Avitus Filter Insert - 8mm, Avitus Filter Insert - 5mm
- K152474 — Avitus Bone Harvester
Data sourced from openFDA. This site is unofficial and independent of the FDA.