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FDA 510(k)

MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY

K-Number: K871822 · 1987-05-26

ApplicantMcconnell Orthopedic
Decision Date1987-05-26
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Mcconnell Orthopedic. It received FDA 510(k) clearance on 1987-05-26 under 510(k) number K871822. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY?

MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY is a medical device that received FDA 510(k) clearance on 1987-05-26. The listed applicant is Mcconnell Orthopedic. The 510(k) number is K871822.

When did MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY receive FDA 510(k) clearance?

MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY received FDA 510(k) clearance on 1987-05-26, under 510(k) number K871822.

Who is the listed applicant for MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY?

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

What is the FDA product code for MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY?

The FDA product code for MCCONNELL ORTHOPEDIC U-HOOK ASSEMBLY is FWZ.

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Other records listing Mcconnell Orthopedic 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.

K910974MCCONNELL SHOULDER BRACEK905564PREP AND OPERATING STANDK905565LATERAL BUTTRESS SUPPORTK885100MCCONNELL REAMER GUIDEK871824MCCONNELL ORTHOPEDIC SUSPENSION SYSTEMK871821MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT

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Related Devices (Code: FWZ)

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.

K960019RETRACTOR ARM CLAMPBiopsys Medical, Inc.K945415'LIL MAC ACCESSORY CLAMP(TM)D.L. Nelson and Assoc., Inc.K944779CARBON LIGHTS HAND SURGERY TABLEAllen Medical Systems, Inc.K935381KAPS POSITIONING ARMAndronic Devices, Ltd.K931037WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)Whitmore Ent., Inc.K926225SPONGE COUNTERAmerican Medical Manufacturer, 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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