ACETABULAR CUP PUSHER/IMPACTOR— 510(k) K885305

Name: FDA 510(k) clearance K885305
Creator: U.S. Food and Drug Administration
Published: 1989-02-08

Substantially Equivalent

Cobot Medical Corp.

FDA 510(k) clearance K885305 for ACETABULAR CUP PUSHER/IMPACTOR, Substantially Equivalent on 1989-02-08. Applicant: Cobot Medical Corp.. Device class: 1.

Clearance details

Applicant: Cobot Medical Corp.
Product code: Code HXO
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1988-12-27
Decision date: 1989-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramus, NJ, US

Download summary PDF View on FDA.gov ↗

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