The following data is part of a premarket notification filed by Medtronic Sofamor Danek, Inc. with the FDA for Perimeter Interbody Fusion Device.
| Device ID | K132700 |
| 510k Number | K132700 |
| Device Name: | PERIMETER INTERBODY FUSION DEVICE |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | MEDTRONIC SOFAMOR DANEK, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
| Contact | Ankit K Shah |
| Correspondent | Ankit K Shah MEDTRONIC SOFAMOR DANEK, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-08-29 |
| Decision Date | 2013-09-26 |
| Summary: | summary |