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FDA 510(k)

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS

K-Number: K000232 · 2000-02-25

ApplicantCorin USA
Decision Date2000-02-25
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2000-02-25 under 510(k) number K000232. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS?

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS is a medical device that received FDA 510(k) clearance on 2000-02-25. The listed applicant is Corin USA. The 510(k) number is K000232.

When did ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS receive FDA 510(k) clearance?

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS received FDA 510(k) clearance on 2000-02-25, under 510(k) number K000232.

Who is the listed applicant for ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS?

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

What is the FDA product code for ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS?

The FDA product code for ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS is JWH.

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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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