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FDA 510(k)

MENISCUS EXTRACTOR

K-Number: K820225 · 1982-02-04

ApplicantOrtho Pared Instruments, Inc.
Decision Date1982-02-04
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MENISCUS EXTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Pared Instruments, Inc.. It received FDA 510(k) clearance on 1982-02-04 under 510(k) number K820225. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENISCUS EXTRACTOR?

MENISCUS EXTRACTOR is a medical device that received FDA 510(k) clearance on 1982-02-04. The listed applicant is Ortho Pared Instruments, Inc.. The 510(k) number is K820225.

When did MENISCUS EXTRACTOR receive FDA 510(k) clearance?

MENISCUS EXTRACTOR received FDA 510(k) clearance on 1982-02-04, under 510(k) number K820225.

Who is the listed applicant for MENISCUS EXTRACTOR?

The FDA 510(k) record lists Ortho Pared Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENISCUS EXTRACTOR?

The FDA product code for MENISCUS EXTRACTOR is HRX.

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Other records listing Ortho Pared Instruments, 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.

K831772GUILLOTINE BLADEK820226UNIVERSALL DRILL GUIDEK812566UNIVERSAL SUTURE PASSER

Related Devices (Code: HRX)

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

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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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