The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Hoffmann Dynamic Wrist Fixator.
Device ID | K910986 |
510k Number | K910986 |
Device Name: | HOFFMANN DYNAMIC WRIST FIXATOR |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Contact | Margaret F Crowe |
Correspondent | Margaret F Crowe HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-07 |
Decision Date | 1992-01-16 |