Parallax Medical, Inc. · Class II · Cleared Jul 18, 2001
| K-number | K011206 |
| Device name | PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES |
| Applicant | Parallax Medical, Inc. |
| Product code | KNW |
| Device class | Class II |
| Decision date | Jul 18, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 876.1075 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov