OSTEO EX-FI-RE— 510(k) K920149

Substantially Equivalent

Osteo AG

FDA 510(k) clearance K920149 for OSTEO EX-FI-RE, Substantially Equivalent on 1992-04-09. Applicant: Osteo AG. Device class: 2.

Clearance details

Applicant: Osteo AG
Product code: Code JEC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1992-01-10
Decision date: 1992-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greenwood, SC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Osteo AG

K933340 — OSTEO INTERLOCKING-COMPRESSION NAIL1994-06-30
K922193 — OSTEO KIRSCHNER WIRE1992-07-23
K922194 — OSTEO STEINMANN PIN1992-07-23
K922195 — OSTEO FEMORAL NAIL1992-07-23
K922196 — OSTEO TIBIA NAIL1992-07-23

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