The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Inc. Unicompartmental And Biocompartmental Knee System Instruments.
Device ID | K113038 |
510k Number | K113038 |
Device Name: | SMITH & NEPHEW INC. UNICOMPARTMENTAL AND BIOCOMPARTMENTAL KNEE SYSTEM INSTRUMENTS |
Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | Gino Rouss |
Correspondent | Gino Rouss SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | HSX |
Subsequent Product Code | KRR |
Subsequent Product Code | NPJ |
CFR Regulation Number | 888.3520 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-10-12 |
Decision Date | 2012-01-05 |
Summary: | summary |