RD 140 SURGICAL BENDER— 510(k) K870084

Name: FDA 510(k) clearance K870084
Creator: U.S. Food and Drug Administration
Published: 1987-01-28

Substantially Equivalent

Terray Manufacturing, Inc.

FDA 510(k) clearance K870084 for RD 140 SURGICAL BENDER, Substantially Equivalent on 1987-01-28. Applicant: Terray Manufacturing, Inc.. Device class: 1.

Clearance details

Applicant: Terray Manufacturing, Inc.
Product code: Code HXW
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1987-01-08
Decision date: 1987-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario K7s 1l8, CA

Download summary PDF View on FDA.gov ↗

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