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FDA 510(k)

SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.

K-Number: K924016 · 1993-12-06

ApplicantSymbiosis Corp.
Decision Date1993-12-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1993-12-06 under 510(k) number K924016. 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 SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.?

SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. is a medical device that received FDA 510(k) clearance on 1993-12-06. The listed applicant is Symbiosis Corp.. The 510(k) number is K924016.

When did SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. receive FDA 510(k) clearance?

SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. received FDA 510(k) clearance on 1993-12-06, under 510(k) number K924016.

Who is the listed applicant for SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.?

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

What is the FDA product code for SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.?

The FDA product code for SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. is HRX.

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Other records listing Symbiosis 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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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

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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