K053155 is an FDA 510(k) clearance for the VIMPLANT. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by Cybermed, Inc. (Seoul, KR). The FDA issued a Cleared decision on November 23, 2005, 9 days after receiving the submission on November 14, 2005.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K053155 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 14, 2005 |
| Decision Date | November 23, 2005 |
| Days to Decision | 9 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LLZ - System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |