LYQ — Accessories, Fixation, Spinal Intervertebral Body Class I

FDA Device Classification

FDA product code LYQ covers "Accessories, Fixation, Spinal Intervertebral Body", a Class I medical device regulated under 21 CFR 888.4540. Submissions are reviewed by the Orthopedic panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LYQ
Device Class
Class I
Regulation Number
888.4540
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K893415rugglesTRANS-ORAL DEPTH GAUGEJune 7, 1989
K883784warsaw orthopedicTSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATEApril 6, 1989
K882871terray manufacturingCASF DRILL GUIDE DG 170September 23, 1988