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FDA 510(k)

OSTEOPORE TCP

K-Number: K062496 · 2006-10-19

ApplicantSpinecraft, Inc.
Decision Date2006-10-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOPORE TCP is the device name listed in this FDA 510(k) record. The listed applicant is Spinecraft, Inc.. It received FDA 510(k) clearance on 2006-10-19 under 510(k) number K062496. 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 OSTEOPORE TCP?

OSTEOPORE TCP is a medical device that received FDA 510(k) clearance on 2006-10-19. The listed applicant is Spinecraft, Inc.. The 510(k) number is K062496.

When did OSTEOPORE TCP receive FDA 510(k) clearance?

OSTEOPORE TCP received FDA 510(k) clearance on 2006-10-19, under 510(k) number K062496.

Who is the listed applicant for OSTEOPORE TCP?

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

What is the FDA product code for OSTEOPORE TCP?

The FDA product code for OSTEOPORE TCP is MQV.

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Other records listing Spinecraft, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K092825APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHERK062513APEX SPINE SYSTEM

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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