The following data is part of a premarket notification filed by Applied Osteo Systems, Inc. with the FDA for True/lok Monolateral/bilateral Fixator.
Device ID | K941048 |
510k Number | K941048 |
Device Name: | TRUE/LOK MONOLATERAL/BILATERAL FIXATOR |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
Applicant | APPLIED OSTEO SYSTEMS, INC. 1243 ALPINE RD. SUITE 221 Walnut Creek, CA 94596 -4370 |
Contact | Scott Huntley |
Correspondent | Scott Huntley APPLIED OSTEO SYSTEMS, INC. 1243 ALPINE RD. SUITE 221 Walnut Creek, CA 94596 -4370 |
Product Code | LXT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-03-07 |
Decision Date | 1994-10-03 |