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FDA 510(k)

MARROWMINER

K-Number: K071732 · 2007-09-24

ApplicantStemcor Systems, Inc.
Decision Date2007-09-24
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARROWMINER is the device name listed in this FDA 510(k) record. The listed applicant is Stemcor Systems, Inc.. It received FDA 510(k) clearance on 2007-09-24 under 510(k) number K071732. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARROWMINER?

MARROWMINER is a medical device that received FDA 510(k) clearance on 2007-09-24. The listed applicant is Stemcor Systems, Inc.. The 510(k) number is K071732.

When did MARROWMINER receive FDA 510(k) clearance?

MARROWMINER received FDA 510(k) clearance on 2007-09-24, under 510(k) number K071732.

Who is the listed applicant for MARROWMINER?

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

What is the FDA product code for MARROWMINER?

The FDA product code for MARROWMINER is GDM.

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Related Devices (Code: GDM)

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.

K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.K923872BONE MARROW BIOPSY SYSTEMThe Straumann Co.

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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