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 |