RESORABPLUG— 510(k) K920118

Substantially Equivalent

Sofamor Danek Mfg., Inc.

FDA 510(k) clearance K920118 for RESORABPLUG, Substantially Equivalent on 1993-02-08. Applicant: Sofamor Danek Mfg., Inc.. Device class: 2.

Clearance details

Applicant: Sofamor Danek Mfg., Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1992-01-13
Decision date: 1993-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

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More clearances from Sofamor Danek Mfg., Inc.

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K932029 — TSRH SPINAL SCREWS1995-01-20
K922486 — DANEK TISSUE CUTTING AND REMOVAL SYSTEM1993-10-12
K930710 — SENTRY POSTERIOR SPINAL SYSTEM1993-10-01

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