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 |