CUTTER, P607 BONE— 510(k) K770305

Substantially Equivalent

Dentronix, Inc.

FDA 510(k) clearance K770305 for CUTTER, P607 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 ↗

Recent devices under product code FZT

K112400 — SMARTSHEARS2011-09-12
K890818 — AUTO SUTURE DISPOSABLE SURGICAL TROCAR*1989-05-04
K872990 — MICRINS SURGICAL SCISSOR1987-08-17
K841741 — SINGLE HAIR TRANSPLANT GRAFT1984-07-23
K841247 — SPC DISPOSABLE CUTTER1984-05-02

More clearances from Dentronix, Inc.

K910202 — DENTRONIX MODEL 20001991-03-13
K880322 — DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM1988-07-13
K771005 — NEW PODIATRY PRODUCTS1977-06-17
K771006 — MODIFIED PODIATRY PRODUCTS1977-06-17
K770302 — CUTTER, P606 BONE1977-03-09

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