The following data is part of a premarket notification filed by Instrument Makar, Inc. with the FDA for Makar Mini Cannulated Cancellous Screws.
Device ID | K912021 |
510k Number | K912021 |
Device Name: | MAKAR MINI CANNULATED CANCELLOUS SCREWS |
Classification | Screw, Fixation, Bone |
Applicant | INSTRUMENT MAKAR, INC. 2950 EAST MT. HOPE RD. Okemos, MI 48864 |
Contact | Keith M Mcgrath |
Correspondent | Keith M Mcgrath INSTRUMENT MAKAR, INC. 2950 EAST MT. HOPE RD. Okemos, MI 48864 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-07 |
Decision Date | 1991-11-22 |