ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.— 510(k) K933059

Name: FDA 510(k) clearance K933059
Creator: U.S. Food and Drug Administration
Published: 1994-06-22

Substantially Equivalent

Jace Systems, Inc.

FDA 510(k) clearance K933059 for ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD., Substantially Equivalent on 1994-06-22. 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: 1993-06-22
Decision date: 1994-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moorestown, NJ, US

Download summary PDF View on FDA.gov ↗

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