Arthrosurface, Inc.
FDA 510(k) & PMA Approved Devices — 21 products
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Total Devices21
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K203375 | OVOMotion Reverse Shoulder Arthroplasty System | PHX | 2021-06-24 | View |
| 510(k) | K200718 | Arthrosurface WristMotion Total Wrist Arthroplasty System | JWJ | 2020-10-15 | View |
| 510(k) | K190261 | BOSS Toe Fixation System | KWD | 2019-08-14 | View |
| 510(k) | K181280 | Patello-Femoral Wave (Kahuna) Arthroplasty System | KRR | 2018-06-14 | View |
| 510(k) | K173964 | OVOMotion Shoulder Arthroplasty System | HSD | 2018-04-18 | View |
| 510(k) | K172383 | Arthrosurface Bone Screws | HWC | 2017-12-22 | View |
| 510(k) | K170440 | KISSloc Suture System | HTN | 2017-05-03 | View |
| 510(k) | K170350 | ToeMATE® Hammertoe Correction System | HWC | 2017-03-03 | View |
| 510(k) | K162391 | AlignMATE™ Lapidus Arthrodesis System | HRS | 2017-02-21 | View |
| 510(k) | K161539 | Arthrosurface Bone Screws | HWC | 2016-06-30 | View |
| 510(k) | K152454 | HemiCAP MTP Resurfacing Hemi-Arthroplasty System | KWD | 2016-04-11 | View |
| 510(k) | K131377 | HEMICAP MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT | KWD | 2013-11-19 | View |
| 510(k) | K130859 | HAMMERTOE CORRECTION SYSTEM | HWC | 2013-07-25 | View |
| 510(k) | K122334 | CHECKMATE SMALL BONE FUSION SYSTEM | HRS | 2012-11-28 | View |
| 510(k) | K113762 | CHECKMATE METATARSO-PHALANGEAL (MTP) ARTHRODESIS SYSTEM | HRS | 2012-02-06 | View |
| 510(k) | K091196 | GRS GLENOID RESURFACING SYSTEM | KWS | 2009-10-27 | View |
| 510(k) | K071413 | HEMICAP PATELLO-FEMORAL RESURFACING SYSTEM | KRR | 2007-11-09 | View |
| 510(k) | K063370 | CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLASTY | KWD | 2007-01-12 | View |
| 510(k) | K060127 | HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS | KRR | 2006-03-16 | View |
| 510(k) | K050373 | UNICAP UNICOMPARTMENTAL KNEE RESURFACING PROSTHESIS | HSX | 2005-10-11 | View |
No matching devices.
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