MINILINE BRACKET— 510(k) K881789

Substantially Equivalent

Alexotek Co.

FDA 510(k) clearance K881789 for MINILINE BRACKET, Substantially Equivalent on 1988-06-01. Applicant: Alexotek Co.. Device class: 1.

Clearance details

Applicant: Alexotek Co.
Product code: Code EJF
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1988-04-26
Decision date: 1988-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eugene, OR, US

Download summary PDF View on FDA.gov ↗

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K923372 — MEMORY WIRE1994-04-22
K933080 — ORTHOTECH DURA-GOLD BARCKETS1994-03-23

More clearances from Alexotek Co.

K834446 — ALEXOTEK LINGUAL TUBES1984-04-05
K834392 — LABIAL CUSPID TUBE1984-02-28
K834272 — ALEXOLOK BRACKET1984-02-03

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