The following data is part of a premarket notification filed by Depuy Spine with the FDA for Depuy Spine Lateral Cage System.
Device ID | K082128 |
510k Number | K082128 |
Device Name: | DEPUY SPINE LATERAL CAGE SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | DEPUY SPINE 325 PARAMOUNT DR. Raynham, MA 02767 |
Contact | Denise Duchene |
Correspondent | Denise Duchene DEPUY SPINE 325 PARAMOUNT DR. Raynham, MA 02767 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-07-29 |
Decision Date | 2008-11-14 |
Summary: | summary |