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

Accessories, Fixation, Spinal Interlaminal

21 CFR 888.3050 / Orthopedic
FDA source (opens on fda.gov)

LYP is the FDA product code for Accessories, Fixation, Spinal Interlaminal, a class II device type, regulated under 21 CFR 888.3050. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LYP
Device name
Accessories, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LYP

By decision year
1 clearance under product code LYP with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LYP by decision year
YearClearances
19891

Applicants with the most clearances

Product code LYP
Applicants holding the most 510(k) clearances under product code LYP
ApplicantClearances
Mizuho Orthopedic Systems Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LYP.