The following data is part of a premarket notification filed by Gs Medical Co., Ltd. with the FDA for Gs Medical Anyplus Peek Lumbar Cages (alif And Dlif).
| Device ID | K111354 |
| 510k Number | K111354 |
| Device Name: | GS MEDICAL ANYPLUS PEEK LUMBAR CAGES (ALIF AND DLIF) |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | GS MEDICAL CO., LTD. 111 HILL ROAD PO BOX 395 Douglassville, PA 19518 |
| Contact | Donald W Guthner |
| Correspondent | Donald W Guthner GS MEDICAL CO., LTD. 111 HILL ROAD PO BOX 395 Douglassville, PA 19518 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-05-13 |
| Decision Date | 2011-10-17 |
| Summary: | summary |