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FDA 510(k)

ORTHOPEDIC FORCEPS

K-Number: K780397 · 1978-03-22

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1978-03-22
Product CodeHTX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-03-22 under 510(k) number K780397. The device is classified under product code HTX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC FORCEPS?

ORTHOPEDIC FORCEPS is a medical device that received FDA 510(k) clearance on 1978-03-22. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780397.

When did ORTHOPEDIC FORCEPS receive FDA 510(k) clearance?

ORTHOPEDIC FORCEPS received FDA 510(k) clearance on 1978-03-22, under 510(k) number K780397.

Who is the listed applicant for ORTHOPEDIC FORCEPS?

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

What is the FDA product code for ORTHOPEDIC FORCEPS?

The FDA product code for ORTHOPEDIC FORCEPS is HTX.

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Other records listing Orthopedic Equipment Co., 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.

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COMK841189OEC/REZAIAN SPINAL FIXATORK800530SCHLEIN TRI-SURFACE ANKLEK781445SPREADERK790247TOURNIQUET TEST GAGEK790209FILTER SYSTEM, ALTNER DISPOSABLE

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Related Devices (Code: HTX)

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.

K874954MANUAL RONGEURSolway, Inc.K841621BACK RADIUS CUTTERPlastafil, Inc.K841620FRONT RADIUS CUTTERPlastafil, Inc.K760325SURGICAL INSTRUMENTS, ORTHOPEDICDepuy, 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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