The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Pushlock.
Device ID | K051219 |
510k Number | K051219 |
Device Name: | PUSHLOCK |
Classification | Fastener, Fixation, Biodegradable, Soft Tissue |
Applicant | ARTHREX, INC. 1370 CREEKSIDE BLVD. Naples, FL 34108 -1945 |
Contact | Sally Foust |
Correspondent | Sally Foust ARTHREX, INC. 1370 CREEKSIDE BLVD. Naples, FL 34108 -1945 |
Product Code | MAI |
Subsequent Product Code | HWC |
Subsequent Product Code | MBI |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-12 |
Decision Date | 2005-06-29 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PUSHLOCK 88597670 not registered Live/Pending |
Jewelex New York, Ltd. 2019-08-29 |
PUSHLOCK 87049897 not registered Dead/Abandoned |
RSP INDUSTRIES INC. 2016-05-25 |
PUSHLOCK 85254213 not registered Dead/Abandoned |
Stanley Logistics, L.L.C. 2011-03-01 |
PUSHLOCK 78596985 3113144 Live/Registered |
Arthrex, Inc. 2005-03-29 |
PUSHLOCK 76000975 2479527 Dead/Cancelled |
AURAFIN LLC 2000-03-15 |