MODEL 9000 AT ANKLE CPM DEVICE— 510(k) K902707

Substantially Equivalent

Sutter Corp.

FDA 510(k) clearance K902707 for MODEL 9000 AT ANKLE CPM DEVICE, Substantially Equivalent on 1990-07-25. Applicant: Sutter Corp.. Device class: 1.

Clearance details

Applicant: Sutter Corp.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1990-06-19
Decision date: 1990-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXB

K072887 — G-TRAINER MEDICAL2008-01-25
K003272 — FLO-BOOT2001-04-04
K952975 — ANKLE CALF EXERCISER PHLEBOPUMP1996-09-25
K953456 — E-Z FLEX1996-01-26
K955105 — BTE CPM-101995-12-29

More clearances from Sutter Corp.

K943354 — SUTTER HAMMERTOE JOINT PROSTHESIS1995-06-12
K945221 — SUTTER MODEL 6000 HAND CPM DEVICE1995-02-27
K931588 — SUTTER PROXIMAL INTERPHALANGEAL JOINT1994-03-10
K924654 — FIRST METATARSOPHALANGEAL JOINT MOTION SPLINT1993-02-22
K914860 — SUTTER MODEL 10000 LEG CPM DEVICE1992-01-08

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