The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Bioabsorbable Interference Screw.
Device ID | K943548 |
510k Number | K943548 |
Device Name: | BIOABSORBABLE INTERFERENCE SCREW |
Classification | Staple, Fixation, Bone |
Applicant | ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
Contact | Frederick Tobia |
Correspondent | Frederick Tobia ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
Product Code | JDR |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-21 |
Decision Date | 1995-03-20 |