ClearanceBrief
510(k) K013860 ยท GDW Staple, Implantable

AUTO SUTURE SURGICAL STAPLES

ApplicantUnited States Surgical, A Division of Tyco Healthc, Norwalk CT, US
DecisionSubstantially Equivalent, Dec 19, 2001
ReceivedNov 21, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K013860

DateFirm and productCodeLinked 510(k)
Jul 20, 2004United States Surgical
Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 30 Reloadable Stapler,Single Patient Use,3.5mm DST Series Ref: TA3035S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 30 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA30348S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 45 Reloadable Stapler,Single Patient Use, 3.5mm DST Series Ref: TA4535S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 45 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA4548S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 60 Reloadable Stapler,Single Patient Use, 3.5mm DST Series Ref: TA6035S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 60 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA6048S
Terminated
GDWNone listed
Jul 20, 2004United States Surgical
Auto SutureTA 90 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA9048S
Terminated
GDWNone listed

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