K172558 is an FDA 510(k) clearance for the iVAS 8g Bone Biopsy Kit, iVAS 11g Bone Biopsy Kit, iVAS 10g Bone Biopsy Kit. This device is classified as a Instrument, Biopsy (Class II - Special Controls, product code KNW).
Submitted by Stryker Corporation (Kalamazoo, US). The FDA issued a Cleared decision on October 5, 2017, 42 days after receiving the submission on August 24, 2017.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K172558 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 24, 2017 |
| Decision Date | October 05, 2017 |
| Days to Decision | 42 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | KNW — Instrument, Biopsy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1075 |