INSERTER, PLUG, BONE, LIDGE— 510(k) K780283

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K780283 for INSERTER, PLUG, BONE, LIDGE, Substantially Equivalent on 1978-03-17. Applicant: Depuy, Inc.. Device class: 1.

Clearance details

Applicant: Depuy, Inc.
Product code: Code LGF
Device class: Class 1
Regulation: 21 CFR 888.5940
Advisory panel: Orthopedic
Date received: 1978-02-21
Decision date: 1978-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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