The following data is part of a premarket notification filed by Extremity Medical Llc with the FDA for Io Fix Hand, Io Fix Foot, Extremity Medical Screw System.
Device ID | K101700 |
510k Number | K101700 |
Device Name: | IO FIX HAND, IO FIX FOOT, EXTREMITY MEDICAL SCREW SYSTEM |
Classification | Screw, Fixation, Bone |
Applicant | EXTREMITY MEDICAL LLC 300 INTERPACE PARKWAY SUITE 410 Parsippany, NJ 07054 |
Contact | Jamy Gannoe |
Correspondent | Jamy Gannoe EXTREMITY MEDICAL LLC 300 INTERPACE PARKWAY SUITE 410 Parsippany, NJ 07054 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-17 |
Decision Date | 2010-10-12 |
Summary: | summary |