Home › Seaspine Orthopedics Corporation › Atoll
Atoll
Seaspine Orthopedics Corporation · Model 16-32-4517 · UDI-DI 10889981034474
1
510(k) clearances
14,609
Adverse events (40 deaths)
68
Recalls
322
Facilities
Description
4.5mm Self Tapping Occipital Screw, 17mm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-02-16 | Medtronic Sofamor Danek USA Inc | Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws |
| 2023-02-16 | Medtronic Sofamor Danek USA Inc | Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws |
| 2023-02-16 | Medtronic Sofamor Danek USA Inc | Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws |
| 2023-02-16 | Medtronic Sofamor Danek USA Inc | Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws |
| 2023-02-16 | Medtronic Sofamor Danek USA Inc | Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws |
| 2022-06-13 | K2M, Inc. | Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irrit |
| 2022-01-13 | K2M, Inc | Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lot |
| 2022-01-13 | K2M, Inc | Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lot |
| 2020-03-26 | Medtronic Sofamor Danek USA Inc | Nonconforming product; length of the product measured shorter than the labeled length. |
| 2020-01-28 | Medicrea International | An internal component was assembled in the incorrect orientation, which may lead to the tulip head disengaging from the crew shank during or after screw insertion, or during the re |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.