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 |