K142442 is an FDA 510(k) clearance for the MAGNA-FX AND MINI MAGNA-FX CANNULATED SCREW FIXATION SYSTEM. This device is classified as a Screw, Fixation, Bone (Class II - Special Controls, product code HWC).
Submitted by Zimmer, Inc. (Warsaw, US). The FDA issued a Cleared decision on October 3, 2014, 31 days after receiving the submission on September 2, 2014.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K142442 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 02, 2014 |
| Decision Date | October 03, 2014 |
| Days to Decision | 31 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HWC — Screw, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |