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 |