K051165 is an FDA 510(k) clearance for the KLS MARTIN STERNAL TALON. This device is classified as a Plate, Fixation, Bone (Class II - Special Controls, product code HRS).
Submitted by KLS-Martin L.P. (Jacksonville, US). The FDA issued a Cleared decision on September 7, 2006, 490 days after receiving the submission on May 5, 2005.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K051165 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 05, 2005 |
| Decision Date | September 07, 2006 |
| Days to Decision | 490 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HRS — Plate, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |