SILVER OSTEOTOME— 510(k) K772374

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K772374 for SILVER OSTEOTOME, Substantially Equivalent on 1978-03-09. Applicant: Edward Weck, Inc..

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code KDG
Advisory panel: General, Plastic Surgery
Date received: 1977-12-27
Decision date: 1978-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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