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FDA 510(k)

ARTHROSTRESS

K-Number: K772321 · 1978-01-03

ApplicantMtd, Inc.
Decision Date1978-01-03
Product CodeJEB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROSTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Mtd, Inc.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772321. The device is classified under product code JEB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSTRESS?

ARTHROSTRESS is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Mtd, Inc.. The 510(k) number is K772321.

When did ARTHROSTRESS receive FDA 510(k) clearance?

ARTHROSTRESS received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772321.

Who is the listed applicant for ARTHROSTRESS?

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

What is the FDA product code for ARTHROSTRESS?

The FDA product code for ARTHROSTRESS is JEB.

Related Clinical Trials

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Other records listing Mtd, 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.

K063439MEDICAL IMAGE MANAGEMENT DEVICES FOR VISION TOOLSK833559ARMBOARDK791374THE MTD VARA SET CASETTE HOLDERK771659PATIENT RESTRAINT SYSTEM

Related Devices (Code: JEB)

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.

K905816ORTHOVISION TABLEAmerican Sterilizer Co.K900405SCHOLTEN FRAMEScholten Surgical Instruments, Inc.K891917ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.K891387WILLIAMS BELT & BOOTArthro-Medic, Inc.K881101K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.K880263OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, Inc.

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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