JACE KNEE EXTENSION SYSTEM -- MODIFICATION— 510(k) K922185

Name: FDA 510(k) clearance K922185
Creator: U.S. Food and Drug Administration
Published: 1992-06-11

Substantially Equivalent

Jace Systems, Inc.

FDA 510(k) clearance K922185 for JACE KNEE EXTENSION SYSTEM -- MODIFICATION, Substantially Equivalent on 1992-06-11. Applicant: Jace Systems, Inc.. Device class: 1.

Clearance details

Applicant: Jace Systems, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1992-05-07
Decision date: 1992-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moorestown, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXB

view all

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 Jace Systems, Inc.

view all

K931016 — JACE MODEL H440 HAND CPM DEVICE1994-06-22
K933059 — ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.1994-06-22
K931781 — JACE TRI-STIM DEVICE1993-10-08
K921351 — JACE MODEL PM-410 HAND CPM DEVICE1992-05-04
K920380 — JACE MODEL W550 WRIST CPM DEVICE1992-02-11

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