ClearanceBrief
510(k) K993021 ยท HRX Arthroscope

METRX SYSTEM

ApplicantSurgical Navigation Technologies, Inc., Broomfield CO, US
DecisionSubstantially Equivalent, Nov 10, 1999
ReceivedSep 8, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993021

DateFirm and productCodeLinked 510(k)
Jul 13, 2005Warsaw Orthopedic, Inc.
Medtronic Sofamor Danek brand METRx System 16 mm Med Procedure Kit; Ref 9560016.
Terminated
HRXNone listed
Jul 13, 2005Warsaw Orthopedic, Inc.
Medtronic Sofamor Danek brand METRx System 18 mm Med Procedure Kit; Ref 9560018.
Terminated
HRXNone listed
Jul 13, 2005Warsaw Orthopedic, Inc.
Medtronic Sofamor Danek brand METRx System MD Procedure Kit; Ref 9560030.
Terminated
HRXNone listed

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