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FDA 510(k)

ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)

K-Number: K873619 · 1988-01-14

ApplicantArthropedics, Inc.
Decision Date1988-01-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K873619. 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 ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)?

ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873619.

When did ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) receive FDA 510(k) clearance?

ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) received FDA 510(k) clearance on 1988-01-14, under 510(k) number K873619.

Who is the listed applicant for ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)?

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

What is the FDA product code for ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)?

The FDA product code for ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) is HRX.

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Other records listing Arthropedics, 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.

K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873653MONOPOLAR CAUTERY BLADE TIP #TM-1701K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873711RETROGRADE KNIFE, DISPOSABLE #TM-1613K873503CUP BIOPSY FORCEPS, LEFT

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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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