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BonOs Inject

OSARTIS GmbH · Model 01-0309 · UDI-DI 04260056883231

NDNLODNKDPML Prescription
10
510(k) clearances
4,809
Adverse events (94 deaths)
86
Recalls
114
Facilities

Description

BonOs® Inject is a radiopaque, injectable bone cement for the treatment of pathological fractures of the vertebral body due to osteoporosis, cancer, or benign lesions using vertebroplasty or balloon kyphoplasty procedure. When used in conjunction with NEO Pedicle Screw System™ BonOs® Inject is intended to restore the integrity of the spinal column even in the absence of fusion for a limited time in patients with advanced stage tumors involving the thoracic and lumbar spine in whom life expectancy is of insufficient duration to permit achievement of fusion. NEO Pedicle Screws augmented with BonOs® Inject Cement are for use at spinal levels where the structural integrity of the spine is not severely compromised. Mixing the two separate sterile components initially produces a ductile, injectable bone cement which, after hardening in situ, is able to stabilize neoplastic vertebral lesions and vertebral compression fractures. BonOs® Inject cement powder also contains insoluble zirconium dioxide as an X-ray contrast medium.

Recalls

DateFirmReason
2022-12-15TEKNIMED SASIncorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.
2021-05-18Stryker SpineThe products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-05-18Stryker SpineThe products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.