The following data is part of a premarket notification filed by Frontier Medical Devices, Inc. with the FDA for Frontier Sadl Interbody Fusion Device.
Device ID | K112700 |
510k Number | K112700 |
Device Name: | FRONTIER SADL INTERBODY FUSION DEVICE |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | FRONTIER MEDICAL DEVICES, INC. 13540 GUILD AVENUE Apple Valley, MN 55124 |
Contact | Rich Jansen |
Correspondent | Rich Jansen FRONTIER MEDICAL DEVICES, INC. 13540 GUILD AVENUE Apple Valley, MN 55124 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-09-16 |
Decision Date | 2012-11-01 |
Summary: | summary |