The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Forza Spacer System, Pillar Peek Spacer System, Pillar Sa Peek Spacer System, Skyhawk Lateral Interbody Fusion System.
| Device ID | K162446 |
| 510k Number | K162446 |
| Device Name: | FORZA Spacer System, PILLAR PEEK Spacer System, PILLAR SA PEEK Spacer System, SKYHAWK Lateral Interbody Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | ORTHOFIX INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Contact | Jacki Koch |
| Correspondent | Jacki Koch ORTHOFIX INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-09-01 |
| Decision Date | 2016-12-22 |
| Summary: | summary |