The following data is part of a premarket notification filed by Consensus Orthopedics, Inc. with the FDA for Cs2 Hip System.
| Device ID | K122512 |
| 510k Number | K122512 |
| Device Name: | CS2 HIP SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | CONSENSUS ORTHOPEDICS, INC. 1115 WINDFIELD WAY STE 100 El Dorado Hills, CA 95762 |
| Contact | Matthew M Hull |
| Correspondent | Matthew M Hull CONSENSUS ORTHOPEDICS, INC. 1115 WINDFIELD WAY STE 100 El Dorado Hills, CA 95762 |
| Product Code | LPH |
| Subsequent Product Code | KWY |
| Subsequent Product Code | LZO |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-17 |
| Decision Date | 2012-11-05 |
| Summary: | summary |