The following data is part of a premarket notification filed by Exactech, Inc. with the FDA for Exatech Acumatch Integrated Hip System C-series Cemented Femoral Stem.
Device ID | K023646 |
510k Number | K023646 |
Device Name: | EXATECH ACUMATCH INTEGRATED HIP SYSTEM C-SERIES CEMENTED FEMORAL STEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
Applicant | EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Contact | Lisa Simpson |
Correspondent | Lisa Simpson EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Product Code | JDI |
CFR Regulation Number | 888.3350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-10-30 |
Decision Date | 2002-11-13 |