FDA Device Intelligence
HomeSeaspine Orthopedics Corporation › Sierra™

Sierra™

Seaspine Orthopedics Corporation · Model 50-5015 · UDI-DI 10889981042998

MNIKWP Prescription
1
510(k) clearances
3,992
Adverse events (17 deaths)
213
Recalls
343
Facilities

Description

Occipital Screw, 15mm. The Sierra occipito-cervico-thoracic (OCT) spinal fixation system, including polyaxial screws, rods, locking caps, occipital plates, occipital screws, lateral connectors, contoured crossbars, hooks, and components, is used to provide stabilization of the spine in order to permit the biological process of spinal fusion to occur. Accepted standard techniques of spinal fusion are an integral part of the implantation of this system.

Recalls

DateFirmReason
2026-02-18XTANT Medical Holdings, IncUnits from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
2023-07-12Medicrea InternationalThere is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
2018-07-05CTL Medical Corporationthe anti-toggle ring of the hex driver may separate from the driver shaft. If this occurs during surgery, the anti-toggle ring can be pressed into the pedicle screw head and cause
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.

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 docs
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.