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FDA 510(k)

NECKTRAC

K-Number: K813017 · 1981-11-25

ApplicantLossing Orthopedic, Inc.
Decision Date1981-11-25
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NECKTRAC is the device name listed in this FDA 510(k) record. The listed applicant is Lossing Orthopedic, Inc.. It received FDA 510(k) clearance on 1981-11-25 under 510(k) number K813017. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NECKTRAC?

NECKTRAC is a medical device that received FDA 510(k) clearance on 1981-11-25. The listed applicant is Lossing Orthopedic, Inc.. The 510(k) number is K813017.

When did NECKTRAC receive FDA 510(k) clearance?

NECKTRAC received FDA 510(k) clearance on 1981-11-25, under 510(k) number K813017.

Who is the listed applicant for NECKTRAC?

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

What is the FDA product code for NECKTRAC?

The FDA product code for NECKTRAC is HST.

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Other records listing Lossing Orthopedic, 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.

K900475DISTRAC(TM) TABLEK864152BACK SAVER LIFT BELT/WHEELCHAIR TRANSFER DEVICEK862874THE TOWERED 90/90 UNITK843581PROM NAIDK840551MOBILIZERK823236BACK ON TRACK INVERSION THERAPY & EXER

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Related Devices (Code: HST)

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.

K162702Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression TableStl International, Inc.K110858LO-BAK TRAXRoland F Berthiaume, DCK984190BACK-ON-TRAC, MODEL 101BOTBack-On-Track, Inc.K872121K AND D HOME TRACTJoseph A. Kott, M.D.K870212ARTHROSCOPIC SHOULDER HOLDERDyonics, Inc.K870125EXTREMITY ELEVATOROrthopedic 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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