The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for S-lif Intervertebral Body Fusion Device.
Device ID | K092815 |
510k Number | K092815 |
Device Name: | S-LIF INTERVERTEBRAL BODY FUSION DEVICE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
Contact | John Sullivan |
Correspondent | John Sullivan SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-09-14 |
Decision Date | 2010-06-30 |
Summary: | summary |