FDA device listing

Klassic Femoral Augment, Distal,Klassic Femoral Augment, Posterior,Klassic Femoral Augment Screw, Distal,Klassic Femoral…

FDA device listing 1213813473 · Total Joint Orthopedics, Inc

Key facts

Proprietary names Klassic Femoral Augment, Distal,Klassic Femoral Augment, Posterior,Klassic Femoral Augment Screw, Distal,Klassic Femoral Augment Screw, Posterior,Klassic Stem Adapter, Femoral,Klassic Stem Extension, Cemented,Klassic Tibial Augment,Universal Cone
Owner/operator Total Joint Orthopedics, Inc
Owner/operator number 10036774
Premarket submissions K230537
Product codes JWH, MBH, OIY
Device names JWH - Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, MBH - Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer, OIY - Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
Device class Class II
Classification regulations (21 CFR) 888.3560, 888.3565
Review panels Orthopedic
Registered establishments TOTAL JOINT ORTHOPEDICS, INC.
Establishment registrations 3008544874
FEI numbers 3008544874
Establishment operations Complaint File Establishment, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 100–999 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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