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FDA 510(k)

PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM

K-Number: K121725 · 2012-11-07

Decision Date2012-11-07
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology, Inc.. It received FDA 510(k) clearance on 2012-11-07 under 510(k) number K121725. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM?

PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM is a medical device that received FDA 510(k) clearance on 2012-11-07. The listed applicant is Pioneer Surgical Technology, Inc.. The 510(k) number is K121725.

When did PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM receive FDA 510(k) clearance?

PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM received FDA 510(k) clearance on 2012-11-07, under 510(k) number K121725.

Who is the listed applicant for PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM?

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

What is the FDA product code for PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM?

The FDA product code for PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM is KWP.

Related Clinical Trials

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.

Other records listing Pioneer Surgical Technology, 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.

View all 22 devices →

Related Devices (Code: KWP)

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.

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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