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FDA 510(k)

C.C.F. FEMORAL DEBRIDEMENT PROBE

K-Number: K790996 · 1979-06-27

ApplicantDepuy, Inc.
Decision Date1979-06-27
Product CodeHTO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

C.C.F. FEMORAL DEBRIDEMENT PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K790996. The device is classified under product code HTO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.C.F. FEMORAL DEBRIDEMENT PROBE?

C.C.F. FEMORAL DEBRIDEMENT PROBE is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Depuy, Inc.. The 510(k) number is K790996.

When did C.C.F. FEMORAL DEBRIDEMENT PROBE receive FDA 510(k) clearance?

C.C.F. FEMORAL DEBRIDEMENT PROBE received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790996.

Who is the listed applicant for C.C.F. FEMORAL DEBRIDEMENT PROBE?

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

What is the FDA product code for C.C.F. FEMORAL DEBRIDEMENT PROBE?

The FDA product code for C.C.F. FEMORAL DEBRIDEMENT PROBE is HTO.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HTO)

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.

K111437SYNTHES RIA SYSTEM (EXPANDED INDICATIONS)Synthes (USA) Products, LLCK042899SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONSSynthes (Usa)K013527MODIFICATION TO SYNTHES (USA) REAMER IRRIGATOR ASPIRATOR (RIA) SYSTEMSynthes (Usa)K993335SYNTHES REAMER/IRRIGATOR/ASPIRATOR (RIA) SYSTEMSynthes (Usa)K954915FLEXIBLE INTRAMEDULLARY REAMERZimmer, Inc.K903248COMBINATION REAMEROnyx Medical Corp.

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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