The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Acufex Biofix Absorbable Fixation Rod-modification.
Device ID | K922766 |
510k Number | K922766 |
Device Name: | ACUFEX BIOFIX ABSORBABLE FIXATION ROD-MODIFICATION |
Classification | Pin, Fixation, Smooth |
Applicant | ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
Contact | Jeffrey Henderson |
Correspondent | Jeffrey Henderson ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
Product Code | HTY |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent - Kit (SESK) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-02 |
Decision Date | 1993-07-09 |