510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LYQClass I

Accessories, Fixation, Spinal Intervertebral Body

21 CFR 888.4540 / Orthopedic
FDA source (opens on fda.gov)

LYQ is the FDA product code for Accessories, Fixation, Spinal Intervertebral Body, a class I device type, regulated under 21 CFR 888.4540. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
LYQ
Device name
Accessories, Fixation, Spinal Intervertebral Body
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
2

Clearances, product code LYQ

By decision year
3 clearances under product code LYQ with a decision year between 1988 and 1989, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LYQ by decision year
YearClearances
19881
19892

Applicants with the most clearances

Product code LYQ
Applicants holding the most 510(k) clearances under product code LYQ
ApplicantClearances
Ruggles Corp.1
Terray Manufacturing, Inc.1
Warsaw Orthopedic, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 21 companies shown, in name order