Biopro, Inc.
FDA 510(k) & PMA Approved Devices — 41 products
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Total Devices41
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K163627 | Shotel Ankle Arthrodesis Nail System | HSB | 2017-09-14 | View |
| 510(k) | K162674 | BioPro Foot Plating Systems | HRS | 2017-06-16 | View |
| 510(k) | K132510 | BIOPRO - INFINITY PLATE ANCHOR SYSTEM | HTN | 2013-10-24 | View |
| 510(k) | K130298 | BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM | JDW | 2013-06-18 | View |
| 510(k) | K121973 | BIOPRO HEMI-EDGE TOE SYSTEM | KWD | 2012-10-30 | View |
| 510(k) | K100761 | BIOPRO POLAR HEAD | KWY | 2010-12-03 | View |
| 510(k) | K101030 | MODIFICATION TO HBS HEADLESS BONE SCREW | HWC | 2010-06-03 | View |
| 510(k) | K090208 | BIOPRO FEMORAL HEADS | JDI | 2009-05-22 | View |
| 510(k) | K083490 | BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685 | HTY | 2009-03-18 | View |
| 510(k) | K082705 | BIOPRO BIPOLAR HEAD, MODELS 18130-18152 | KWY | 2008-12-15 | View |
| 510(k) | K081149 | BIOPRO GO-EZ SCREW | HWC | 2008-08-05 | View |
| 510(k) | K072298 | BIOPRO MEMORY STAPLE, MODELS 18062-18073 | JDR | 2007-10-29 | View |
| 510(k) | K061798 | BIOPRO MEMORY STAPLE | JDR | 2006-08-21 | View |
| 510(k) | K061089 | MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599 | KYI | 2006-06-20 | View |
| 510(k) | K052596 | MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507 | KYI | 2005-11-15 | View |
| 510(k) | K043542 | BIOPRO TARA FEMORAL RESURFACING COMPONENT | KXA | 2005-05-18 | View |
| 510(k) | K041595 | TOE MP JOINT, MODELS 10412-10414, 14958, 14960, 1060-10062,16818,-16822,16867-16870 | KWD | 2004-11-12 | View |
| 510(k) | K041936 | BIOPRO SUBTALAR IMPLANT | HWC | 2004-09-08 | View |
| 510(k) | K011460 | WUJIN #3 TIBIAL BONE PLATE | HRS | 2001-08-07 | View |
| 510(k) | K011459 | WUJIN #3 FEMORAL BONE PLATE | HRS | 2001-08-07 | View |
No matching devices.
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