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FDA 510(k)

HOLLYWOOD, PACIFICA, REDONDO, VENTURA

K-Number: K082310 · 2008-11-10

ApplicantSeaspine, Inc.
Decision Date2008-11-10
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOLLYWOOD, PACIFICA, REDONDO, VENTURA is the device name listed in this FDA 510(k) record. The listed applicant is Seaspine, Inc.. It received FDA 510(k) clearance on 2008-11-10 under 510(k) number K082310. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLLYWOOD, PACIFICA, REDONDO, VENTURA?

HOLLYWOOD, PACIFICA, REDONDO, VENTURA is a medical device that received FDA 510(k) clearance on 2008-11-10. The listed applicant is Seaspine, Inc.. The 510(k) number is K082310.

When did HOLLYWOOD, PACIFICA, REDONDO, VENTURA receive FDA 510(k) clearance?

HOLLYWOOD, PACIFICA, REDONDO, VENTURA received FDA 510(k) clearance on 2008-11-10, under 510(k) number K082310.

Who is the listed applicant for HOLLYWOOD, PACIFICA, REDONDO, VENTURA?

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

What is the FDA product code for HOLLYWOOD, PACIFICA, REDONDO, VENTURA?

The FDA product code for HOLLYWOOD, PACIFICA, REDONDO, VENTURA is MAX.

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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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