ARTHROPHONOMETER— 510(k) K862286

Substantially Equivalent

Arthrotek, Inc.

FDA 510(k) clearance K862286 for ARTHROPHONOMETER, Substantially Equivalent on 1987-01-07. Applicant: Arthrotek, Inc.. Device class: 1.

Clearance details

Applicant: Arthrotek, Inc.
Product code: Code NFQ
Device class: Class 1
Regulation: 21 CFR 872.2050
Advisory panel: Dental
Date received: 1986-06-16
Decision date: 1987-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Hartford, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NFQ

K970116 — ESG-1 ELECTROSONOGRAM (ESG-1)1997-04-02
K905657 — SONOPAK/QS, SONOPAK1991-05-15
K905449 — ELECTROSONOGRAM ESG-11991-04-26

More clearances from Arthrotek, Inc.

K061776 — ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE2006-09-25
K061801 — 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS2006-08-07
K061657 — HITCH LACTOSORB SUTURE ANCHOR2006-07-25
K061389 — ALLTHREAD LACTOSORB SUTURE ANCHOR2006-07-19
K060693 — MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR2006-06-06

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