510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001476Substantially Equivalent

Torque Instrument, Model 8500

Spinalight Inc, Kennesaw GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001476 is the FDA 510(k) clearance record for TORQUE INSTRUMENT, MODEL 8500, cleared for Spinalight, Inc. on under FDA product code LXM (Manipulator, Plunger-Like Joint). FDA records list 7 510(k) clearances for Spinalight, Inc., from to . As of , FDA records show no recalls naming K001476.

Clearance record

Decision date
Received
(85 days to decision)
Product code
LXM Manipulator, Plunger-Like Joint
Device class
Unclassified
Review panel
Unknown
Applicant
Spinalight, Inc. 1620 Albritton Dr., Kennesaw GA
510(k) summary
Statement
Third party review
No

Clearances, product code LXM

Trailing 12 months

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

FDA records show no clearances under product code LXM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXM, 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