The following data is part of a premarket notification filed by Safe Orthopaedics with the FDA for Sterispine Lc Cage.
Device ID | K151756 |
510k Number | K151756 |
Device Name: | STERISPINE LC CAGE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | SAFE ORTHOPAEDICS Parc Des Bellevues Allee R. Luxembourg-Bat. Californie Eragny Sur Oise, FR 95610 |
Contact | Pierre Dumouchel |
Correspondent | Pierre Dumouchel SAFE ORTHOPAEDICS Parc Des Bellevues Allee R. Luxembourg-Bat. Californie Eragny Sur Oise, FR 95610 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-29 |
Decision Date | 2015-08-21 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
03760219913047 | K151756 | 000 |