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 |