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FDA 510(k)

PINN-ACL CROSSPIN

K-Number: K043106 · 2005-01-19

ApplicantLinvatec Corp.
Decision Date2005-01-19
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PINN-ACL CROSSPIN is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 2005-01-19 under 510(k) number K043106. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINN-ACL CROSSPIN?

PINN-ACL CROSSPIN is a medical device that received FDA 510(k) clearance on 2005-01-19. The listed applicant is Linvatec Corp.. The 510(k) number is K043106.

When did PINN-ACL CROSSPIN receive FDA 510(k) clearance?

PINN-ACL CROSSPIN received FDA 510(k) clearance on 2005-01-19, under 510(k) number K043106.

Who is the listed applicant for PINN-ACL CROSSPIN?

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

What is the FDA product code for PINN-ACL CROSSPIN?

The FDA product code for PINN-ACL CROSSPIN is HTY.

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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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