The following data is part of a premarket notification filed by Novastep with the FDA for Nexis Osteosynthesis Compressive Screws.
Device ID | K143229 |
510k Number | K143229 |
Device Name: | Nexis Osteosynthesis Compressive Screws |
Classification | Screw, Fixation, Bone |
Applicant | NOVASTEP Espace Performance Alphasis - Batiment C1-C2 Saint Gregoire, FR 35769 |
Contact | Gilles Audic |
Correspondent | Gilles Audic NOVASTEP Espace Performance Alphasis - Batiment C1-C2 Saint Gregoire, FR 35769 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-10 |
Decision Date | 2015-02-06 |
Summary: | summary |