SCHULTZ METACARPAL COMPONENT DRIVER
K-Number: K870848 · 1987-03-13
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Device Summary
Frequently Asked Questions
What is the SCHULTZ METACARPAL COMPONENT DRIVER?
SCHULTZ METACARPAL COMPONENT DRIVER is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K870848.
When did SCHULTZ METACARPAL COMPONENT DRIVER receive FDA 510(k) clearance?
SCHULTZ METACARPAL COMPONENT DRIVER received FDA 510(k) clearance on 1987-03-13, under 510(k) number K870848.
Who is the listed applicant for SCHULTZ METACARPAL COMPONENT DRIVER?
The FDA 510(k) record lists Warsaw Orthopedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCHULTZ METACARPAL COMPONENT DRIVER?
The FDA product code for SCHULTZ METACARPAL COMPONENT DRIVER is HWR.
Related Clinical Trials
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.
Other records listing Warsaw Orthopedic, 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.
Related Devices (Code: HWR)
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.
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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