ClearanceBrief
510(k) K203381 ยท HWC Screw, Fixation, Bone

Dynanail Mini Hybrid

ApplicantMedShape, Inc., Atlanta GA, US
DecisionSubstantially Equivalent, Jan 15, 2021
ReceivedNov 17, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203381

DateFirm and productCodeLinked 510(k)
Nov 17, 2021Medshape, INC.
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Open, Classified
HWCNone listed

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