FDA 510(k)

PERMA FACIAL IMPLANTS

K-Number: K071823 · 2007-09-19

Decision Date2007-09-19

Product CodeODU

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PERMA FACIAL IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Surgisil. It received FDA 510(k) clearance on 2007-09-19 under 510(k) number K071823. The device is classified under product code ODU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERMA FACIAL IMPLANTS?

PERMA FACIAL IMPLANTS is a medical device that received FDA 510(k) clearance on 2007-09-19. The listed applicant is Surgisil. The 510(k) number is K071823.

When did PERMA FACIAL IMPLANTS receive FDA 510(k) clearance?

PERMA FACIAL IMPLANTS received FDA 510(k) clearance on 2007-09-19, under 510(k) number K071823.

Who is the listed applicant for PERMA FACIAL IMPLANTS?

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

What is the FDA product code for PERMA FACIAL IMPLANTS?

The FDA product code for PERMA FACIAL IMPLANTS is ODU.

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Official Source

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