ClearanceBrief
510(k) K021351 ยท HWC Screw, Fixation, Bone

BIOSTEON CROSS PIN

ApplicantBiocomposites, Ltd., Stoke On Trent, GB
DecisionSubstantially Equivalent, Oct 17, 2002
ReceivedApr 29, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021351

DateFirm and productCodeLinked 510(k)
Nov 18, 2005Stryker Endoscopy
Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-350; Product is distributed by Stryker Endoscopy, 5900 Optical Court, San Jose, CA 95138
Terminated
HWCNone listed

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