K961522 is an FDA 510(k) clearance for the KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN. This device is classified as a Pin, Fixation, Smooth (Class II - Special Controls, product code HTY).
Submitted by Synvasive Technology, Inc. (El Dorado, US). The FDA issued a Cleared decision on September 23, 1996, 154 days after receiving the submission on April 22, 1996.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K961522 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 22, 1996 |
| Decision Date | September 23, 1996 |
| Days to Decision | 154 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HTY — Pin, Fixation, Smooth |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |