The following data is part of a premarket notification filed by Renovis Surgical Technologies, Llc with the FDA for Renovis Surgical Hip Joint Replacement Prosthesis.
| Device ID | K112897 |
| 510k Number | K112897 |
| Device Name: | RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS |
| Classification | Hip Prosthesis, Semi-constrained, Cemented, Metal/polymer, + Additive, Porous, Uncemented |
| Applicant | RENOVIS SURGICAL TECHNOLOGIES, LLC 825 NICOLLET MALL STE 1820 Minneapolis, MN 55402 |
| Contact | David A Teicher |
| Correspondent | David A Teicher RENOVIS SURGICAL TECHNOLOGIES, LLC 825 NICOLLET MALL STE 1820 Minneapolis, MN 55402 |
| Product Code | OQG |
| Subsequent Product Code | LPH |
| Subsequent Product Code | LZO |
| Subsequent Product Code | OQI |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-10-03 |
| Decision Date | 2012-06-13 |
| Summary: | summary |