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 |