BETA
Developer and manufacturer of proprietary cervical fusion implants and fixation systems.
SpineNet is a Florida-based spinal-device company that evolved from distribution into proprietary implant development, manufacturing and commercialization. Its portfolio includes the SSP single-screw anterior cervical plate and ACC anterior cervical cage.
The business uses specialist engineering, manufacturing and regulatory resources alongside its commercial organization. FDA records support separate SSP and anterior cervical cage decisions; the earlier cage record uses the Daytona trade name, which FDA’s recall record links to SpineNet ACC.
Founding president King Floyd leads the company with COO Bill McDonald. Two reviewed 2013 recalls concern specific historical cage labeling and a marrow-aspiration needle kit; both are terminated and are kept separate from current portfolio counts.
SpineNet’s SSP and ACC systems have matched 510(k) records. Its historical recall entries are retained with their original affected products and status rather than generalized to every current device. [12][14][2][3][13][1]
The matched FDA history contains 2 distinct recall events: 0 open, 2 terminated. Z-2103-2013 (2013-02-05; terminated): The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing. Z-2107-2013 (2013-02-04; terminated): SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval. [8][7]
Latest recorded source review: 2026-10-20.
Documented commercial product families.
Single-screw anterior cervical plate with integrated instrumentation. [14][16]
FDA-clearedCommercially offered; exact model and country availability should be confirmed with the manufacturer.
Anterior cervical cage; earlier FDA record uses Daytona name. [14][15]
FDA-clearedCommercially offered; exact model and country availability should be confirmed with the manufacturer.
Historical needle kit retained solely to explain a scoped recall. [14]
Commercial availability not establishedCurrent availability not established.
Accessed 10/20/2026