← Back to catalogue

Klassic Knee System - Klassic Knee PS-Post Femur - Klassic Knee Tibial Insert, PS-Post, E-Link Poly

FDA 510(k)

Class II (US FDA 510(k))

510(k) K183596

by Total Joint Orthopedics, Inc.

Identifiers

510(k) Number
K183596 FDA 510(k)
FDA Product Code
JWH FDA 510(k)
Models / Variants
Klassic Knee Tibial Insert, PS-Post, E-Link Poly FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 888.3560 FDA 510(k)
Regulation Number
888.3560 FDA 510(k)
Advisory Committee
Orthopedic FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Klassic Knee System - Klassic Knee PS-Post Femur - Klassic Knee Tibial Insert, PS-Post, E-Link Poly by Total Joint Orthopedics, Inc. — Class II — FDA_510K…

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA 510(k) K183596 24 fields · synced Jun 18, 2026