BONE PAD REMOVER— 510(k) K910225

Substantially Equivalent

Acra Cut, Inc.

FDA 510(k) clearance K910225 for BONE PAD REMOVER, Substantially Equivalent on 1991-02-12. Applicant: Acra Cut, Inc.. Device class: 1.

Clearance details

Applicant: Acra Cut, Inc.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1991-01-18
Decision date: 1991-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Acton, MA, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.