The following data is part of a premarket notification filed by Sulzer Orthopedics, Inc. with the FDA for Natural-knee Ii System-durasul Tibial Insert And Durasul All-poly Patella.
Device ID | K002335 |
510k Number | K002335 |
Device Name: | NATURAL-KNEE II SYSTEM-DURASUL TIBIAL INSERT AND DURASUL ALL-POLY PATELLA |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
Contact | Mitchell Dhority |
Correspondent | Mitchell Dhority SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-08-01 |
Decision Date | 2000-10-25 |