510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883130Substantially Equivalent

Biomechanics Force Platform/# Or6-5-1000 & 2000

Advanced Mechanical Technology Inc, Newton CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883130 is the FDA 510(k) clearance record for BIOMECHANICS FORCE PLATFORM/# OR6-5-1000 & 2000, a class I device, cleared for Advanced Mechanical Technology, Inc. on under FDA product code KHX (Platform, Force-Measuring). FDA records list 5 510(k) clearances for Advanced Mechanical Technology, Inc., from to . As of , FDA records show no recalls naming K883130.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KHX Platform, Force-Measuring
Regulation
21 CFR 890.1575
Device class
Class I
Review panel
Physical Medicine
Applicant
Advanced Mechanical Technology, Inc. 151 California St., Newton CA
Third party review
No

Clearances, product code KHX

Trailing 12 months

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

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