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Novo Surgical Inc.

NOVO SURGICAL, INC. · Model N6923-41CC · UDI-DI 00842331174452

HTX Prescription
5
510(k) clearances
618
Adverse events (2 deaths)
7
Recalls
330
Facilities

Description

ceramic cut micro kerrison detachable rongeur, 40 degrees up, small handles, 9.0 mm opening, black ceramic coat, thin footplate, 1.0 mm bite, 9" (23.0 cm)

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-
2017-05-25Exactech, Inc.Instructions for use (IFU) is updated to clarify the proper technique and instrumentation to ream the Glenoid, i.e., to include a caution statement that the surgeon should ream on-

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.