The following data is part of a premarket notification filed by Medacta International Sa with the FDA for Pao Cortical Screw.
Device ID | K211435 |
510k Number | K211435 |
Device Name: | PAO Cortical Screw |
Classification | Screw, Fixation, Bone |
Applicant | Medacta International SA Strada Regina Castel San Pietro, CH Ch-6874 |
Contact | Stefano Baj |
Correspondent | Chris Lussier Medacta USA 3973 Delp Street Memphis, TN 83118 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-05-10 |
Decision Date | 2021-08-06 |