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FDA 510(k)

NOVOS-NAIL Limb Lengthening System (LLS)

K-Number: K163653 · 2017-10-13

ApplicantSmith & Nephew
Decision Date2017-10-13
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NOVOS-NAIL Limb Lengthening System (LLS) is a medical device manufactured by Smith & Nephew. It received FDA 510(k) clearance on 2017-10-13 under approval number K163653. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVOS-NAIL Limb Lengthening System (LLS)?

NOVOS-NAIL Limb Lengthening System (LLS) is a medical device that received FDA 510(k) clearance on 2017-10-13. It is manufactured by Smith & Nephew. The 510(k) number is K163653.

When was NOVOS-NAIL Limb Lengthening System (LLS) approved by the FDA?

NOVOS-NAIL Limb Lengthening System (LLS) received FDA 510(k) clearance on 2017-10-13, under approval number K163653.

What company makes NOVOS-NAIL Limb Lengthening System (LLS)?

NOVOS-NAIL Limb Lengthening System (LLS) is manufactured by Smith & Nephew.

What is the FDA product code for NOVOS-NAIL Limb Lengthening System (LLS)?

The FDA product code for NOVOS-NAIL Limb Lengthening System (LLS) is HSB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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