ClearanceBrief
510(k) K894184 ยท JDN Implant, Fixation Device, Spinal

BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM

ApplicantBiedermann Motech GmbH, Vs-Schwenningen, DE
DecisionSubstantially Equivalent for Some Indications, Apr 25, 1990
ReceivedJun 16, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894184

No recall in the FDA data names this 510(k).

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