Dyonics, Inc.
FDA 510(k) & PMA Approved Devices — 19 products
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Total Devices19
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K900070 | MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM | HRX | 1990-02-16 | View |
| 510(k) | K896416 | DYONICS SHOULDER PORTAL SYSTEM | HRX | 1990-01-02 | View |
| 510(k) | K893136 | SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY | HRX | 1989-12-14 | View |
| 510(k) | K890665 | MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES | HRX | 1989-11-03 | View |
| 510(k) | K894728 | DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFE | HRX | 1989-08-18 | View |
| 510(k) | K892062 | PS3500 ARTHROSCOPIC SURGICAL SYSTEM | HRX | 1989-06-23 | View |
| 510(k) | K884839 | MODIFIED SAW BLADES TO THE SAGITAL SAW | KIJ | 1988-12-07 | View |
| 510(k) | K881876 | DYNAMIC CRUCIATE TESTER | LYH | 1988-11-17 | View |
| 510(k) | K880739 | DYONICS DRILL GUIDE/ISOMETER SYSTEM | LXI | 1988-03-21 | View |
| 510(k) | K880150 | PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEM | HWE | 1988-03-04 | View |
| 510(k) | K870212 | ARTHROSCOPIC SHOULDER HOLDER | HST | 1987-02-20 | View |
| 510(k) | K862017 | ARTHROSCOPIC SHOULDER LIGAMENT REPAIR KIT | HRX | 1986-12-15 | View |
| 510(k) | K843121 | GUIDE TO THE KNEE | BWN | 1984-09-07 | View |
| 510(k) | K833943 | MENISCAL SUTURING SYSTEM | LXH | 1984-02-27 | View |
| 510(k) | K833587 | DISPOSABLE ARTHROSCOPY BLADE | HRX | 1983-11-14 | View |
| 510(k) | K820367 | INTRA-ARTICULAR SURGICAL SYSTEM | KIJ | 1982-05-07 | View |
| 510(k) | K812506 | THE ARTHROFILE | HTR | 1981-09-24 | View |
| 510(k) | K790502 | DYONICS STEROTOXIC POSITIONER | HAW | 1979-04-05 | View |
| 510(k) | K771218 | INTRA-ARTICULAR SHAVER | KIJ | 1978-02-01 | View |
No matching devices.
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