K130298 is an FDA 510(k) clearance for the BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM. This device is classified as a Pin, Fixation, Threaded (Class II - Special Controls, product code JDW).
Submitted by Biopro, Inc. (Prior Lake, US). The FDA issued a Cleared decision on June 18, 2013, 131 days after receiving the submission on February 7, 2013.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K130298 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 07, 2013 |
| Decision Date | June 18, 2013 |
| Days to Decision | 131 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | JDW — Pin, Fixation, Threaded |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |