K161876 is an FDA 510(k) clearance for the Tritium® Sternal Cable Plate System. This device is classified as a Cerclage, Fixation (Class II - Special Controls, product code JDQ).
Submitted by Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.) (Marquette, US). The FDA issued a Cleared decision on September 9, 2016, 63 days after receiving the submission on July 8, 2016.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3010.
| 510(k) Number | K161876 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 08, 2016 |
| Decision Date | September 09, 2016 |
| Days to Decision | 63 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | JDQ - Cerclage, Fixation |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3010 |