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FDA 510(k)

SPLINT, COCKUP

K-Number: K770890 · 1977-05-26

ApplicantOrthopedic Systems, Inc.
Decision Date1977-05-26
Product CodeIQM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPLINT, COCKUP is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1977-05-26 under 510(k) number K770890. The device is classified under product code IQM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLINT, COCKUP?

SPLINT, COCKUP is a medical device that received FDA 510(k) clearance on 1977-05-26. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K770890.

When did SPLINT, COCKUP receive FDA 510(k) clearance?

SPLINT, COCKUP received FDA 510(k) clearance on 1977-05-26, under 510(k) number K770890.

Who is the listed applicant for SPLINT, COCKUP?

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

What is the FDA product code for SPLINT, COCKUP?

The FDA product code for SPLINT, COCKUP is IQM.

Related Clinical Trials

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Other records listing Orthopedic Systems, 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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910736JACKSON MULTIPURPOSE OPERATING TABLEK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEE

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Related Devices (Code: IQM)

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.

K771287FINGEO EXTENSION SPLINTSFred Sammons, Inc.K770891SPLINH, FOREARMOrthopedic 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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