The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Perimeter Interbody Fusion Device.
Device ID | K090353 |
510k Number | K090353 |
Device Name: | PERIMETER INTERBODY FUSION DEVICE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Lee Grant |
Correspondent | Lee Grant MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-02-11 |
Decision Date | 2009-09-29 |
Summary: | summary |