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

Monitor, Spine Curvature

Unknown
FDA source (opens on fda.gov)

LZW is the FDA product code for Monitor, Spine Curvature. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LZW
Device name
Monitor, Spine Curvature
Device class
Unclassified
Review panel
Unknown
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code LZW

By decision year
5 clearances under product code LZW with a decision year between 1989 and 2010, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LZW by decision year
YearClearances
19891
19901
19951
20091
20101

Applicants with the most clearances

Product code LZW
Applicants holding the most 510(k) clearances under product code LZW
ApplicantClearances
Bagrad1
Dan Kline1
Mcdowell Ent., Inc.1
Perseus Althetics,Llc1
Peter Fischer1

Companies listing this code with FDA

Companies whose registered establishments list this code