The following data is part of a premarket notification filed by Osseus Fusion Systems, Llc with the FDA for Aries® Lumbar Interbodies.
Device ID | K181347 |
510k Number | K181347 |
Device Name: | Aries® Lumbar Interbodies |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
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 | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-05-21 |
Decision Date | 2018-08-15 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
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