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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K121502

SYNTHES CURVILINEAR DISTRACTION SYSTEM · Synthes, Inc. · decided 2012-08-23 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)04.500.240Synthes GmbHMQN10887587016863
(unnamed)04.500.241Synthes GmbHMQN10887587016870
(unnamed)04.500.230Synthes GmbHMQN10887587016849
(unnamed)04.500.218Synthes GmbHMQN10887587016832
(unnamed)04.500.231Synthes GmbHMQN10887587016856
(unnamed)04.500.271Synthes GmbHMQN10887587016917
(unnamed)04.500.201Synthes GmbHMQN10887587016825
(unnamed)04.500.200Synthes GmbHMQN10887587016818
(unnamed)04.500.250Synthes GmbHMQN10887587016887
(unnamed)04.500.251Synthes GmbHMQN10887587016894
(unnamed)04.500.270Synthes GmbHMQN10887587016900