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 |