PHOENIX BONE SCREWS PBS-TYPE SERIES— 510(k) K930125

Name: FDA 510(k) clearance K930125
Creator: U.S. Food and Drug Administration
Published: 1993-12-30

Substantially Equivalent

Phoenix Bioengineering, Inc.

FDA 510(k) clearance K930125 for PHOENIX BONE SCREWS PBS-TYPE SERIES, Substantially Equivalent on 1993-12-30. Applicant: Phoenix Bioengineering, Inc.. Device class: 2.

Clearance details

Applicant: Phoenix Bioengineering, Inc.
Product code: Code HXA
Device class: Class 2
Regulation: 21 CFR 888.3025
Advisory panel: Orthopedic
Date received: 1993-01-12
Decision date: 1993-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bridgeport, PA, US

Download summary PDF View on FDA.gov ↗

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