Biopro, Inc. · Class II · Cleared Nov 15, 2005
| K-number | K052596 |
| Device name | MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507 |
| Applicant | Biopro, Inc. |
| Product code | KYI |
| Device class | Class II |
| Decision date | Nov 15, 2005 |
| Decision | Substantially Equivalent |
| Regulation | 888.3770 |
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