ClearanceBrief
510(k) K020480 ยท KGS Retention Device, Suture

RBM

ApplicantSmith & Nephew, Inc., Mansfield MA, US
DecisionSubstantially Equivalent, Mar 12, 2002
ReceivedFeb 13, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020480

DateFirm and productCodeLinked 510(k)
Apr 26, 2006Smith & Nephew, Inc. Endoscopy Division
FAST-FIX AB Curved Needle Delivery System, Used for meniscal repair. Product Number: 7209399
Terminated
KGSNone listed

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