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FDA 510(k)

B2C HIP SYSTEM

K-Number: K992490 · 1999-08-19

ApplicantLepine Groupe Spa.
Decision Date1999-08-19
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

B2C HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lepine Groupe Spa.. It received FDA 510(k) clearance on 1999-08-19 under 510(k) number K992490. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B2C HIP SYSTEM?

B2C HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-19. The listed applicant is Lepine Groupe Spa.. The 510(k) number is K992490.

When did B2C HIP SYSTEM receive FDA 510(k) clearance?

B2C HIP SYSTEM received FDA 510(k) clearance on 1999-08-19, under 510(k) number K992490.

Who is the listed applicant for B2C HIP SYSTEM?

The FDA 510(k) record lists Lepine Groupe Spa. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B2C HIP SYSTEM?

The FDA product code for B2C HIP SYSTEM is JDI.

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Related Devices (Code: JDI)

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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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