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FDA 510(k)

MACMED PAEDIATRIC INTRAMEDULLARY NAIL

K-Number: K991877 · 1999-08-06

ApplicantInnervision, Inc.
Decision Date1999-08-06
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MACMED PAEDIATRIC INTRAMEDULLARY NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Innervision, Inc.. It received FDA 510(k) clearance on 1999-08-06 under 510(k) number K991877. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACMED PAEDIATRIC INTRAMEDULLARY NAIL?

MACMED PAEDIATRIC INTRAMEDULLARY NAIL is a medical device that received FDA 510(k) clearance on 1999-08-06. The listed applicant is Innervision, Inc.. The 510(k) number is K991877.

When did MACMED PAEDIATRIC INTRAMEDULLARY NAIL receive FDA 510(k) clearance?

MACMED PAEDIATRIC INTRAMEDULLARY NAIL received FDA 510(k) clearance on 1999-08-06, under 510(k) number K991877.

Who is the listed applicant for MACMED PAEDIATRIC INTRAMEDULLARY NAIL?

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

What is the FDA product code for MACMED PAEDIATRIC INTRAMEDULLARY NAIL?

The FDA product code for MACMED PAEDIATRIC INTRAMEDULLARY NAIL is JDS.

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Other records listing Innervision, 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.

K992345CHRISTOUDIAS SLIM TIP ELECTRODE INSERTK982428CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)K940731INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPESK940750INNERVISION,INC. LAPAROSCOPIC ELECTRODESK940718INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS

Related Devices (Code: JDS)

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.

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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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