ClearanceBrief
510(k) K050210 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

DISPOSABLE CEMENT SPACER MOLDS FOR TEMPORARY KNEE PROSTHESES

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 19, 2005
ReceivedJan 28, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050210

DateFirm and productCodeLinked 510(k)
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Femoral Cement Spacer Mold, 60 MM, Silicone, Sterile, Item 432160.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Femoral Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 432175.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175.
Terminated
JWHNone listed
Apr 3, 2020Biomet, Inc.
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180.
Terminated
JWHNone listed

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