INTERMEDICS ORTHOPEDICS REAMERS— 510(k) K931733

Name: FDA 510(k) clearance K931733
Creator: U.S. Food and Drug Administration
Published: 1994-01-26

Substantially Equivalent

Intermedics Orthopedics

FDA 510(k) clearance K931733 for INTERMEDICS ORTHOPEDICS REAMERS, Substantially Equivalent on 1994-01-26. Applicant: Intermedics Orthopedics. Device class: 1.

Clearance details

Applicant: Intermedics Orthopedics
Product code: Code HTP
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1993-04-07
Decision date: 1994-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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