K053579 is an FDA 510(k) clearance for the COLUMBUS ULTRA CONGRUENT (UC) TIBIAL INSERT/GLIDING SURFACE. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).
Submitted by Aesculap, Inc. (Center Valley, US). The FDA issued a Cleared decision on May 17, 2006, 146 days after receiving the submission on December 22, 2005.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3560.
| 510(k) Number | K053579 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 22, 2005 |
| Decision Date | May 17, 2006 |
| Days to Decision | 146 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | JWH — Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3560 |