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FDA 510(k)

ACE 100 DEGREES TUBULAR PLATE

K-Number: K920738 · 1992-07-27

Decision Date1992-07-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE 100 DEGREES TUBULAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Ace Orthopedic Manufacturing Co.. It received FDA 510(k) clearance on 1992-07-27 under 510(k) number K920738. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE 100 DEGREES TUBULAR PLATE?

ACE 100 DEGREES TUBULAR PLATE is a medical device that received FDA 510(k) clearance on 1992-07-27. The listed applicant is Ace Orthopedic Manufacturing Co.. The 510(k) number is K920738.

When did ACE 100 DEGREES TUBULAR PLATE receive FDA 510(k) clearance?

ACE 100 DEGREES TUBULAR PLATE received FDA 510(k) clearance on 1992-07-27, under 510(k) number K920738.

Who is the listed applicant for ACE 100 DEGREES TUBULAR PLATE?

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

What is the FDA product code for ACE 100 DEGREES TUBULAR PLATE?

The FDA product code for ACE 100 DEGREES TUBULAR PLATE is HRS.

Related Clinical Trials

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.

Other records listing Ace Orthopedic Manufacturing Co. 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.

View all 14 devices →

Related Devices (Code: HRS)

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.

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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