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FDA 510(k)

SPLINT WOOD

K-Number: K832144 · 1983-08-01

ApplicantVermont Wood Industries, Inc.
Decision Date1983-08-01
Product CodeILH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPLINT WOOD is the device name listed in this FDA 510(k) record. The listed applicant is Vermont Wood Industries, Inc.. It received FDA 510(k) clearance on 1983-08-01 under 510(k) number K832144. The device is classified under product code ILH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLINT WOOD?

SPLINT WOOD is a medical device that received FDA 510(k) clearance on 1983-08-01. The listed applicant is Vermont Wood Industries, Inc.. The 510(k) number is K832144.

When did SPLINT WOOD receive FDA 510(k) clearance?

SPLINT WOOD received FDA 510(k) clearance on 1983-08-01, under 510(k) number K832144.

Who is the listed applicant for SPLINT WOOD?

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

What is the FDA product code for SPLINT WOOD?

The FDA product code for SPLINT WOOD is ILH.

Related Clinical Trials

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Related Devices (Code: ILH)

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.

K831548SPLINTSFred Sammons, Inc.K823647FINGER EXTENSION SPLINTFred Sammons, Inc.K823644FINGER FLEXION SPLINTFred Sammons, Inc.K823666UNIVERSAL WRIST SPLINT & FOREARM SPLINTWarm & Form, Orthopedic MaterialsK823601WRIST SUPPORTFred Sammons, Inc.K823393STAX FINGER SPLINTSOrthopedic Systems, Inc.

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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