510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093553Substantially Equivalent

Posturetek

Perseus Althetics,Llc, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093553 is the FDA 510(k) clearance record for POSTURETEK, cleared for Perseus Althetics,Llc on under FDA product code LZW (Monitor, Spine Curvature). FDA records list one 510(k) clearance for Perseus Althetics,Llc. As of , FDA records show no recalls naming K093553.

Clearance record

Decision date
Received
(269 days to decision)
Product code
LZW Monitor, Spine Curvature
Device class
Unclassified
Review panel
Unknown
Applicant
Perseus Althetics,Llc 1425 K St., NW, Suite 1100, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LZW

Trailing 12 months

FDA records hold no clearances under product code LZW in the trailing twelve months.

FDA records show no clearances under product code LZW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LZW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260