SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP
K-Number: K870842 · 1987-05-27
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Device Summary
Frequently Asked Questions
What is the SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP?
SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP is a medical device that received FDA 510(k) clearance on 1987-05-27. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K870842.
When did SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP receive FDA 510(k) clearance?
SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP received FDA 510(k) clearance on 1987-05-27, under 510(k) number K870842.
Who is the listed applicant for SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP?
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 PHALANGEAL COMP RASP/METACARPAL COMP RASP?
The FDA product code for SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP is HTP.
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: HTP)
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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