The following data is part of a premarket notification filed by Newclip Technics with the FDA for Large Screws Range.
Device ID | K160617 |
510k Number | K160617 |
Device Name: | Large Screws Range |
Classification | Screw, Fixation, Bone |
Applicant | NEWCLIP TECHNICS PA De La Lande Saint Martin-45 Rue Des Garottieres Haute-goulaine, FR 44 115 |
Contact | Gaelle Lussori |
Correspondent | J.d. Webb The OrthoMedix Group, Inc. 1001 Oakwood Boulevard Round Rock, TX 78681 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-03 |
Decision Date | 2016-06-03 |
Summary: | summary |