Arthrosurface, Inc.
FDA 510(k) & PMA Approved Produkte — 11 products
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Produkte insgesamt11
Kategorien0
Neueste FDA-Entscheidung
| Typ | Nummer | Produktname | Code | Datum | Aktionen |
|---|---|---|---|---|---|
| 510(k) | K203375 | OVOMotion Reverse Shoulder Arthroplasty System | PHX | 2021-06-24 | Anzeigen |
| 510(k) | K200718 | Arthrosurface WristMotion Total Wrist Arthroplasty System | JWJ | 2020-10-15 | Anzeigen |
| 510(k) | K190261 | BOSS Toe Fixation System | KWD | 2019-08-14 | Anzeigen |
| 510(k) | K181280 | Patello-Femoral Wave (Kahuna) Arthroplasty System | KRR | 2018-06-14 | Anzeigen |
| 510(k) | K173964 | OVOMotion Shoulder Arthroplasty System | HSD | 2018-04-18 | Anzeigen |
| 510(k) | K172383 | Arthrosurface Bone Screws | HWC | 2017-12-22 | Anzeigen |
| 510(k) | K170440 | KISSloc Suture System | HTN | 2017-05-03 | Anzeigen |
| 510(k) | K170350 | ToeMATE® Hammertoe Correction System | HWC | 2017-03-03 | Anzeigen |
| 510(k) | K162391 | AlignMATE® Lapidus Arthrodesis System | HRS | 2017-02-21 | Anzeigen |
| 510(k) | K161539 | Arthrosurface Bone Screws | HWC | 2016-06-30 | Anzeigen |
| 510(k) | K152454 | HemiCAP MTP Resurfacing Hemi-Arthroplasty System | KWD | 2016-04-11 | Anzeigen |
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