The following data is part of a premarket notification filed by Synthes Usa with the FDA for Synthes Variable Angle Lcp Elbow System.
| Device ID | K120070 |
| 510k Number | K120070 |
| Device Name: | SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | SYNTHES USA 1301 GOSHEN PKWY West Chester, PA 19380 |
| Contact | Angela F Lassandro |
| Correspondent | Angela F Lassandro SYNTHES USA 1301 GOSHEN PKWY West Chester, PA 19380 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-01-09 |
| Decision Date | 2012-03-21 |
| Summary: | summary |