K051229 is an FDA 510(k) clearance for the PROFIX FLEX CRUCIATE RETAINING ARTICULAR INSERT. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).
Submitted by Smith & Nephew, Inc. (Memphis, US). The FDA issued a Cleared decision on July 20, 2005, 68 days after receiving the submission on May 13, 2005.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3560.
| 510(k) Number | K051229 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 13, 2005 |
| Decision Date | July 20, 2005 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| 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 |