← Back to catalogue

Foot and Hand Motion

FDA 510(k)

Class II (US FDA 510(k))

510(k) K170012

by Newclip Technics

Identifiers

510(k) Number
K170012 FDA 510(k)
FDA Product Code
HWC FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 888.3040 FDA 510(k)
Regulation Number
888.3040 FDA 510(k)
Advisory Committee
Orthopedic FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Foot and Hand Motion by Newclip Technics — Class II — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (0 countries)

Regulatory Authorizations

No authorizations listed.

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Newclip Technics

Sources (1)

  • FDA 510(k) K170012 24 fields · synced Jun 1, 2026