Class Class II

Synthes Patient Specific Implants (K243715)

K243715 2025-11-12 Traditional
Home/ Devices/ Synthes Patient Specific Implants…

Description

Synthes Patient Specific Implants by Synthes GmbH, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243715
Clearance Date2025-11-12
Clearance TypeTraditional
Product CodeGXN
Regulation Number882.5330

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top