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Dakota ALIF System

PRECISION SPINE, INC. · Model 69-AV-0813-2C · UDI-DI 00840019963787

KWQ Prescription
10
510(k) clearances
10,584
Adverse events (59 deaths)
214
Recalls
364
Facilities

Description

42X 30X 13mm X 8° PEEK-2C

Recalls

DateFirmReason
2026-02-20Clariance-SASDue to a quality issue regarding the presence of burr on the finished cervical plate product.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.
2021-04-26Alphatec Spine, Inc.There is a potential for the screw blocking mechanism on the anterior cervical plate system to disassociate intraoperatively/postoperatively or unlock postoperatively.

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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.