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FDA 510(k)

PERFECTA PS REVISION STEM

K-Number: K962267 · 1996-09-10

ApplicantWrightmedicaltechnologyinc
Decision Date1996-09-10
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

PERFECTA PS REVISION STEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1996-09-10 under 510(k) number K962267. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PERFECTA PS REVISION STEM?

PERFECTA PS REVISION STEM is a medical device that received FDA 510(k) clearance on 1996-09-10. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K962267.

When did PERFECTA PS REVISION STEM receive FDA 510(k) clearance?

PERFECTA PS REVISION STEM received FDA 510(k) clearance on 1996-09-10, under 510(k) number K962267.

Who is the listed applicant for PERFECTA PS REVISION STEM?

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

What is the FDA product code for PERFECTA PS REVISION STEM?

The FDA product code for PERFECTA PS REVISION STEM is JDI.

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Related Devices (Code: JDI)

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

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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