The following data is part of a premarket notification filed by Accel Spine with the FDA for Oracle Lumbar Intervertebral Body Fusion Cage System.
Device ID | K121567 |
510k Number | K121567 |
Device Name: | ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | ACCEL SPINE 14850 Quorum Dr Ste 220 Dallas, TX 75254 |
Contact | Daniel Chon |
Correspondent | Daniel Chon ACCEL SPINE 14850 Quorum Dr Ste 220 Dallas, TX 75254 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-05-29 |
Decision Date | 2012-09-26 |
Summary: | summary |