Sutter Corp.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K943354 | SUTTER HAMMERTOE JOINT PROSTHESIS | KWH | 1995-06-12 | View |
| 510(k) | K945221 | SUTTER MODEL 6000 HAND CPM DEVICE | BXB | 1995-02-27 | View |
| 510(k) | K931588 | SUTTER PROXIMAL INTERPHALANGEAL JOINT | KYJ | 1994-03-10 | View |
| 510(k) | K924654 | FIRST METATARSOPHALANGEAL JOINT MOTION SPLINT | BXB | 1993-02-22 | View |
| 510(k) | K914860 | SUTTER MODEL 10000 LEG CPM DEVICE | BXB | 1992-01-08 | View |
| 510(k) | K902707 | MODEL 9000 AT ANKLE CPM DEVICE | BXB | 1990-07-25 | View |
| 510(k) | K890607 | SUTTER HOSPITAL CPM | BXB | 1989-02-27 | View |
No matching devices.
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