The following data is part of a premarket notification filed by Gs Medical Co., Ltd. with the FDA for Anyplus; Alif Peek Cages, Plif Peek Cages, T-plif Peek Cages, Tlif Peek Cages.
| Device ID | K131612 |
| 510k Number | K131612 |
| Device Name: | ANYPLUS; ALIF PEEK CAGES, PLIF PEEK CAGES, T-PLIF PEEK CAGES, TLIF PEEK CAGES |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | GS MEDICAL CO., LTD. 111 HILL ROAD Douglassville, PA 19518 |
| Contact | Donald W Guthner |
| Correspondent | Donald W Guthner GS MEDICAL CO., LTD. 111 HILL ROAD Douglassville, PA 19518 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-06-03 |
| Decision Date | 2014-04-18 |
| Summary: | summary |