ARTHROSTRESS— 510(k) K772321

Substantially Equivalent

Mtd, Inc.

FDA 510(k) clearance K772321 for ARTHROSTRESS, Substantially Equivalent on 1978-01-03. Applicant: Mtd, Inc.. Device class: 1.

Clearance details

Applicant: Mtd, Inc.
Product code: Code JEB
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1977-12-19
Decision date: 1978-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JEB

K905816 — ORTHOVISION TABLE1991-03-06
K900405 — SCHOLTEN FRAME1990-03-01
K891917 — ORTHO-J, INC. BEK-JS-0041989-05-26
K891387 — WILLIAMS BELT & BOOT1989-05-23
K881101 — K ORTHOPEDIC TABLE1988-04-06

More clearances from Mtd, Inc.

K063439 — MEDICAL IMAGE MANAGEMENT DEVICES FOR VISION TOOLS2007-01-22
K833559 — ARMBOARD1984-01-03
K791374 — THE MTD VARA SET CASETTE HOLDER1979-09-07
K771659 — PATIENT RESTRAINT SYSTEM1977-09-30

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