Abc-1000 Small Joint Reamers

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K862933 ↗

FDA Product Code

HTO

Device Class

Class I

Regulation

21 CFR Part 888.4540

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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• Sg-066 Oxygen Enrichment Kit

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• Ms-303-Oxygen Regulator Shield

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• Flex Arm Be 122, Clamp 122-27

  Class I

  FDA 510(k) K770631 Active Cleared 23 May 1977

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