PAVLIK HARNESS— 510(k) K780375

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K780375 for PAVLIK HARNESS, Substantially Equivalent on 1978-03-15. Applicant: Biomet, Inc.. Device class: 1.

Clearance details

Applicant: Biomet, Inc.
Product code: Code IOZ
Device class: Class 1
Regulation: 21 CFR 890.3665
Advisory panel: Physical Medicine
Date received: 1978-03-08
Decision date: 1978-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.