K110400 is an FDA 510(k) clearance for the TAPERLOC COMPLETE MICROPLASTY STEM. This device is classified as a Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) (Class III - Premarket Approval, product code KWA).
Submitted by Biomet Manufacturing Corp (Warsaw, US). The FDA issued a Cleared decision on September 30, 2011, 231 days after receiving the submission on February 11, 2011.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3330.
| 510(k) Number | K110400 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 11, 2011 |
| Decision Date | September 30, 2011 |
| Days to Decision | 231 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | KWA — Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) |
| Device Class | Class III - Premarket Approval |
| CFR Regulation | 21 CFR 888.3330 |