PACP
K-Number: K083663 · 2009-02-25
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Device Summary
Frequently Asked Questions
What is the PACP?
PACP is a medical device that received FDA 510(k) clearance on 2009-02-25. The listed applicant is Pioneer Surgical Technology. The 510(k) number is K083663.
When did PACP receive FDA 510(k) clearance?
PACP received FDA 510(k) clearance on 2009-02-25, under 510(k) number K083663.
Who is the listed applicant for PACP?
The FDA 510(k) record lists Pioneer Surgical Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PACP?
The FDA product code for PACP is KWQ.
Other records listing Pioneer Surgical Technology 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.
Related Devices (Code: KWQ)
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
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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