The following data is part of a premarket notification filed by Intuitive Spine, Llc with the FDA for Discovery.
Device ID | K111484 |
510k Number | K111484 |
Device Name: | DISCOVERY |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | INTUITIVE SPINE, LLC 33490 PIN OAK PARKWAY Avon Lake, OH 44012 |
Contact | Jennifer Palinchik |
Correspondent | Jennifer Palinchik INTUITIVE SPINE, LLC 33490 PIN OAK PARKWAY Avon Lake, OH 44012 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-05-31 |
Decision Date | 2011-09-12 |
Summary: | summary |