FDA 510(k) Applications for Medical Device Product Code "KGS"
(Retention Device, Suture)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K030031 | ACCU-SPEED, INCORPORATED | SOFT TISSUE ANCHORING WASHERS | 01/28/2003 |
| K964935 | SMITH & NEPHEW ENDOSCOPY, INC. | SUTURE LOCK | 02/25/1997 |
| K020480 | SMITH & NEPHEW, INC. | RBM | 03/12/2002 |
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