ClearanceBrief
510(k) K173882 ยท NKB Thoracolumbosacral Pedicle Screw System

SeaSpine Mariner Pedicle Screw System

ApplicantSeaSpine Orthopedics Corporation, Carlsbad CA, US
DecisionSubstantially Equivalent, Feb 6, 2018
ReceivedDec 21, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173882

DateFirm and productCodeLinked 510(k)
Jul 20, 2026SEASPINE ORTHOPEDICS CORPORATION
SeaSpine Polyaxial Head REF Number: 41-3010
Open, Classified
NKBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.