The following data is part of a premarket notification filed by Gs Medical Co., Ltd. with the FDA for Anyplus Peek Cages.
Device ID | K100516 |
510k Number | K100516 |
Device Name: | ANYPLUS PEEK CAGES |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | GS MEDICAL CO., LTD. 111 HILL ROAD PO BOX 395 Douglassville, PA 19818 |
Contact | Donald W Guthner |
Correspondent | Donald W Guthner GS MEDICAL CO., LTD. 111 HILL ROAD PO BOX 395 Douglassville, PA 19818 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-02-23 |
Decision Date | 2010-12-03 |
Summary: | summary |