The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Depuy Attune Knee System.
Device ID | K101433 |
510k Number | K101433 |
Device Name: | DEPUY ATTUNE KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer + Additive/metal/polymer + Additive |
Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Contact | Kathy Boggs |
Correspondent | Kathy Boggs DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Product Code | OIY |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-05-21 |
Decision Date | 2010-12-10 |
Summary: | summary |