ClearanceBrief
510(k) K090132 ยท HRX Arthroscope

MAXMORESPINE SPINAL SYSTEM

ApplicantHoogland Spine Products, GmbH, Muenchen, DE
DecisionSubstantially Equivalent, Jun 9, 2009
ReceivedJan 21, 2009
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K090132

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.