The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Acufex Cannulated Screws, Washers, Bone Plates.
Device ID | K890641 |
510k Number | K890641 |
Device Name: | ACUFEX CANNULATED SCREWS, WASHERS, BONE PLATES |
Classification | Plate, Fixation, Bone |
Applicant | ACUFEX MICROSURGICAL, INC. 575 UNIVERSITY AVE. Norwood, MA 02062 |
Contact | Richard E Franko |
Correspondent | Richard E Franko ACUFEX MICROSURGICAL, INC. 575 UNIVERSITY AVE. Norwood, MA 02062 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-02-08 |
Decision Date | 1989-02-27 |