Intellijoint Surgical, Inc.
Intellijoint Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2021, with 2 FDA device recalls on record.
Top product codes for Intellijoint Surgical, Inc.
FDA recalls by Intellijoint Surgical, Inc.
- Z-1559-2020 — Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation System is a computer-controlled, optical localizer intended to provide intra-operative measurements to a surgeon to aid in selection and positioning of orthopedic implant system components, where a reference to a rigid anatomical structure can be identified.
- Z-2228-2019 — Workstation, G2, Configured (P/N 000-0241)
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 Intellijoint Surgical, Inc.
- K211876 — Intellijoint VIEW
- K191507 — Intellijoint® Navigation System
- K172849 — Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray
- K171525 — Intellijoint HIP Generation 2B System
- K162364 — Intellijoint HIP Generation 2A System
- K151364 — Intellijoint HIP(tm) System
- K133759 — INTELLIJOINT HIP
Data sourced from openFDA. This site is unofficial and independent of the FDA.