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FDA 510(k)

ANTERIOR CRUCIATE LIGAMENT GRASPER

K-Number: K841241 · 1985-02-06

ApplicantSurgical Products Corp.
Decision Date1985-02-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR CRUCIATE LIGAMENT GRASPER is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Products Corp.. It received FDA 510(k) clearance on 1985-02-06 under 510(k) number K841241. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTERIOR CRUCIATE LIGAMENT GRASPER?

ANTERIOR CRUCIATE LIGAMENT GRASPER is a medical device that received FDA 510(k) clearance on 1985-02-06. The listed applicant is Surgical Products Corp.. The 510(k) number is K841241.

When did ANTERIOR CRUCIATE LIGAMENT GRASPER receive FDA 510(k) clearance?

ANTERIOR CRUCIATE LIGAMENT GRASPER received FDA 510(k) clearance on 1985-02-06, under 510(k) number K841241.

Who is the listed applicant for ANTERIOR CRUCIATE LIGAMENT GRASPER?

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

What is the FDA product code for ANTERIOR CRUCIATE LIGAMENT GRASPER?

The FDA product code for ANTERIOR CRUCIATE LIGAMENT GRASPER is HRX.

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Other records listing Surgical Products Corp. 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.

K921671SURGILASE FIBERLASE VCO2 LASER WAVEGUIDEK861614GHI WET PENCILK841328SPC ARTHROSCOPY TABLEK841247SPC DISPOSABLE CUTTERK834434MACH I ELECTROSURGERY HAND CONTROL

Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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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