The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Acufex Suretac.
| Device ID | K931519 |
| 510k Number | K931519 |
| Device Name: | ACUFEX SURETAC |
| Classification | Staple, Fixation, Bone |
| Applicant | ACUFEX MICROSURGICAL, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
| Contact | Fred Tobia |
| Correspondent | Fred 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 | 1993-03-26 |
| Decision Date | 1994-06-16 |