The following data is part of a premarket notification filed by Acufex Microsurgical, Inc. with the FDA for Acufex Patellar Bone Block Sizer.
Device ID | K944500 |
510k Number | K944500 |
Device Name: | ACUFEX PATELLAR BONE BLOCK SIZER |
Classification | Arthroscope |
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 | HRX |
CFR Regulation Number | 888.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-09-14 |
Decision Date | 1995-06-12 |