K-CAP-I ORTHOPEDIC FIXATION WIRE CAP— 510(k) K902053

Name: FDA 510(k) clearance K902053
Creator: U.S. Food and Drug Administration
Published: 1990-09-14

Substantially Equivalent

Westcon Orthopedics, Inc.

FDA 510(k) clearance K902053 for K-CAP-I ORTHOPEDIC FIXATION WIRE CAP, Substantially Equivalent on 1990-09-14. Applicant: Westcon Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Westcon Orthopedics, Inc.
Product code: Code LYT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1990-05-07
Decision date: 1990-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Three Bridges, NJ, US

Download summary PDF View on FDA.gov ↗

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