The following data is part of a premarket notification filed by Gs Medical Co., Ltd. with the FDA for Any Plus Spinal Fixation System.
| Device ID | K091717 |
| 510k Number | K091717 |
| Device Name: | ANY PLUS SPINAL FIXATION SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | GS MEDICAL CO., LTD. 220 RIVER ROAD Claremont, NH 03743 |
| Contact | William F Greenrose |
| Correspondent | William F Greenrose GS MEDICAL CO., LTD. 220 RIVER ROAD Claremont, NH 03743 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-06-11 |
| Decision Date | 2010-01-25 |
| Summary: | summary |