The following data is part of a premarket notification filed by Extremity Medical Llc with the FDA for Io Fix, Io Fix Plus, Carpalfix, Extremity Medical Screw And Washer.
Device ID | K121349 |
510k Number | K121349 |
Device Name: | IO FIX, IO FIX PLUS, CARPALFIX, EXTREMITY MEDICAL SCREW AND WASHER |
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 | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-05-04 |
Decision Date | 2012-07-18 |
Summary: | summary |