The following data is part of a premarket notification filed by Osseus Fusion Systems, Llc with the FDA for White Pearl Preferred Angle Anterior Cervical Plate.
Device ID | K160522 |
510k Number | K160522 |
Device Name: | White Pearl Preferred Angle Anterior Cervical Plate |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | OSSEUS FUSION SYSTEMS, LLC 2703 MOCKINGBIRD LANE, SUITE 102 Dallas, TX 75235 |
Contact | Robert Pace |
Correspondent | J. D. Webb THE ORTHOMEDIX GROUP, INC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-25 |
Decision Date | 2016-04-26 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
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