ClearanceBrief
510(k) K020885 ยท HSB Rod, Fixation, Intramedullary And Accessories

FASSIRE-DUVAL TELESCOPIC IM SYSTEM

ApplicantPega Medical, Inc., Quebec, CA
DecisionSubstantially Equivalent, Feb 6, 2003
ReceivedMar 18, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020885

DateFirm and productCodeLinked 510(k)
Apr 29, 2015Pega Medical Inc.
Female Driver, Part number FDr101, instrument used for the insertion of the Fassier-Duval IM Telescopic System. For orthopedic procedures. This instrument is included in the Fassier-Duval IM Teles
Terminated
HSBNone listed
Apr 18, 2014Pega Medical Inc.
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.
Terminated
HSBNone listed
Apr 10, 2014Pega Medical Inc.
Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft), Part number: M040-SS-110; Used in Implant Catalogue number: FD-040(LS)-SS. orthopedic intramedullary rod.
Terminated
HSBNone listed
Mar 2, 2011Pega Medical Inc.
Male Driver 4.0mm (catalog # MDr140L) and Male Driver 3.2mm (catalog # MDr132L), an instrument used for the insertion of the Fassier-Duval Telescopic IM System intramedullary nail, for bone fixation.
Terminated
HSBNone listed

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