The following data is part of a premarket notification filed by Depuy Acromed with the FDA for Isola Band Clamp.
Device ID | K010972 |
510k Number | K010972 |
Device Name: | ISOLA BAND CLAMP |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
Contact | Lisa Gilman |
Correspondent | Lisa Gilman DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-04-02 |
Decision Date | 2001-06-12 |