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 |