ClearanceBrief
510(k) K122160 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

VANGUARD XP KNEE SYSTEM

ApplicantBiomet Manufacturing Corp, Warsaw IN, US
DecisionSubstantially Equivalent, Mar 20, 2013
ReceivedJul 20, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122160

DateFirm and productCodeLinked 510(k)
Aug 15, 2019Zimmer Biomet, Inc.
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 63 mm Item # 195245
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 65 mm Item # 195246
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 67 mm Item # 195247
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 69 mm Item # 195248
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 71 mm Item # 195249
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 73 mm Item # 195250
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 75 mm Item # 195251
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 79 mm Item # 195252
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 83 mm Item # 195253
Terminated
JWHNone listed
Aug 15, 2019Zimmer Biomet, Inc.
Vanguard XP Tibial Tray 87 mm Item # 195254
Terminated
JWHNone listed

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