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FDA 510(k)

BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375

K-Number: K873651 · 1987-11-02

ApplicantArthropedics, Inc.
Decision Date1987-11-02
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375 is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873651. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375?

BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375 is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873651.

When did BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375 receive FDA 510(k) clearance?

BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375 received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873651.

Who is the listed applicant for BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375?

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 BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375?

The FDA product code for BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375 is HXB.

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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.

K873619ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873653MONOPOLAR CAUTERY BLADE TIP #TM-1701K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873711RETROGRADE KNIFE, DISPOSABLE #TM-1613

View all 29 devices →

Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K943472COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK890227SURGICAL PROBEKinetic Medical ProductsK873652HOOK PROBE #TM-1376Arthropedics, Inc.K863149BOWEN PROBEBowen & Company, 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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