K031714 is an FDA 510(k) clearance for the INION TRINION BIODEGRADABLE MENISCUS SCREW. This device is classified as a Screw, Fixation, Bone (Class II - Special Controls, product code HWC).
Submitted by Inion , Ltd. (Tampere, FI). The FDA issued a Cleared decision on August 16, 2004, 441 days after receiving the submission on June 2, 2003.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K031714 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 02, 2003 |
| Decision Date | August 16, 2004 |
| Days to Decision | 441 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 |