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FDA 510(k)

OSTEOPLAST, MODEL POP200

K-Number: K991854 · 1999-08-26

ApplicantInterpore Cross Intl.
Decision Date1999-08-26
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOPLAST, MODEL POP200 is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 1999-08-26 under 510(k) number K991854. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEOPLAST, MODEL POP200?

OSTEOPLAST, MODEL POP200 is a medical device that received FDA 510(k) clearance on 1999-08-26. The listed applicant is Interpore Cross Intl.. The 510(k) number is K991854.

When did OSTEOPLAST, MODEL POP200 receive FDA 510(k) clearance?

OSTEOPLAST, MODEL POP200 received FDA 510(k) clearance on 1999-08-26, under 510(k) number K991854.

Who is the listed applicant for OSTEOPLAST, MODEL POP200?

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

What is the FDA product code for OSTEOPLAST, MODEL POP200?

The FDA product code for OSTEOPLAST, MODEL POP200 is MQV.

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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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