The following data is part of a premarket notification filed by Exactech, Inc. with the FDA for Exactech Equinoxe Shoulder System.
Device ID | K042021 |
510k Number | K042021 |
Device Name: | EXACTECH EQUINOXE SHOULDER SYSTEM |
Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
Applicant | EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Contact | Gary Miller |
Correspondent | Gary Miller EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Product Code | KWS |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-07-28 |
Decision Date | 2004-10-26 |
Summary: | summary |