K080111 is an FDA 510(k) clearance for the ARTHREX COMPRESSION STAPLE. This device is classified as a Staple, Fixation, Bone (Class II - Special Controls, product code JDR).
Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on February 13, 2008, 28 days after receiving the submission on January 16, 2008.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K080111 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 16, 2008 |
| Decision Date | February 13, 2008 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | JDR — Staple, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |