BONE-DRI SURGICAL SPONGE— 510(k) K803125

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K803125 for BONE-DRI SURGICAL SPONGE, Substantially Equivalent on 1981-01-15. Applicant: Howmedica Corp.. Device class: 1.

Clearance details

Applicant: Howmedica Corp.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1980-12-12
Decision date: 1981-01-15
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.