The following data is part of a premarket notification filed by Rootloc Co., Ltd. with the FDA for Acculoc Total Knee System.
Device ID | K182370 |
510k Number | K182370 |
Device Name: | Acculoc Total Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | RootLoc Co., Ltd. #1206, 1210, 68, Digital-ro 9-gil, Geumcheon-gu Seoul, KR 08512 |
Contact | Jungsun Ha |
Correspondent | Jungsun Ha RootLoc Co., Ltd. #1206, 1210, 68, Digital-ro 9-gil, Geumcheon-gu Seoul, KR 08512 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-31 |
Decision Date | 2018-09-27 |
Summary: | summary |