The following data is part of a premarket notification filed by Synthes (usa) with the FDA for Synthes Carniofacial Plate And Screw System.
Device ID | K050608 |
510k Number | K050608 |
Device Name: | SYNTHES CARNIOFACIAL PLATE AND SCREW SYSTEM |
Classification | Plate, Bone |
Applicant | SYNTHES (USA) 1302 WRIGHTS LANE EAST West Chester, PA 19380 |
Contact | Sheri L Musgnung |
Correspondent | Sheri L Musgnung SYNTHES (USA) 1302 WRIGHTS LANE EAST West Chester, PA 19380 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-03-10 |
Decision Date | 2005-05-18 |
Summary: | summary |