CUTTER, P606 BONE— 510(k) K770302

Substantially Equivalent

Dentronix, Inc.

FDA 510(k) clearance K770302 for CUTTER, P606 BONE, Substantially Equivalent on 1977-03-09. Applicant: Dentronix, Inc.. Device class: 1.

Clearance details

Applicant: Dentronix, Inc.
Product code: Code FZT
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-02-16
Decision date: 1977-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K771006 — MODIFIED PODIATRY PRODUCTS1977-06-17
K770303 — NIPPER, NAIL, P610 ENGLISH1977-03-09

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