Surgicraft , Ltd.
10 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE (K091207) | Surgicraft , Ltd. | 2011-02-15 |
| SURGICRAFT SURGICAL MESH SYSTEM (K072370) | Surgicraft , Ltd. | 2008-07-24 |
| SURGICRAFT SCREW FIXATION SYSTEM (K080447) | Surgicraft , Ltd. | 2008-06-13 |
| STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM (K073109) | Surgicraft , Ltd. | 2008-06-04 |
| STALIF (TM) C (K072415) | Surgicraft , Ltd. | 2008-01-25 |
| STALIF TT (K051027) | Surgicraft , Ltd. | 2005-06-29 |
| STALIF TT (K041617) | Surgicraft , Ltd. | 2004-09-08 |
| TITANIUM HARTSHILL SYSTEM (K991662) | Surgicraft , Ltd. | 1999-11-08 |
| THE BONE TIE (K982719) | Surgicraft , Ltd. | 1998-09-25 |
| RANSFORD CERVICAL FIXATION SYSTEM (K965221) | Surgicraft , Ltd. | 1997-08-07 |
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