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510(k) K123342

Device
OPTETRAK LOGIC CRC TIBIAL INSERT
Applicant
EXACTECH, INC.
510(k) number
K123342
Product code
JWH  
Decision
Substantially Equivalent (SESE)
Decision date
2013-01-10
Date received
2012-10-31
Regulation
888.3560
Classification name
Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
PATRICK HUGHES
Address
2320 NW 66th Ct. Gainesville FL US 32653 32653

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code JWH  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K261032NovoKnee (SteriKnee)NovoSource2026-04-27
K253793Materialise TKA Guide SystemMaterialise NV2026-01-06
K252974EMPOWR KneeEncore Medical L.P.2025-12-19
K253197ATTUNE™ Total Knee System; ATTUNE™ Revision Sleeve LPS™ Femoral AdaptorsDepuy Ireland UC2025-11-19
K253314Freedom Infinia™ Total Knee SystemMaxx Orthopedics, Inc.2025-10-29
K253144Freedom® Total Knee System – Titan PCK ComponentsMaxx Orthopedics, Inc.2025-10-22
K252725Stem Extension Line (U2 Total Knee System—PSA Type)United Orthopedic Corporation2025-09-25
K251554Materialise TKA Guide SystemMaterialise NV2025-07-14
K251776EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)Encore Medical L.P.2025-07-08
K251241EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)Encore Medical L.P.2025-07-02
K251717Freedom® Total Knee System – Titanium Tibial Base PlateMaxx Orthopedics, Inc.2025-06-26
K242410NextStep Arthropedix Total Knee SystemNextstep Arthropedix2025-05-08
K250889EXULT Knee Replacement SystemCorentec Co., Ltd.2025-04-17
K250677LEGION Total Knee SystemSmith & Nephew, Inc.2025-04-02
K243991Klassic Knee System - Revision Tibial BaseplateTotal Joint Othopedics, Inc.2025-03-24

Legacy Summary#

summary

FDA Review#

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