Atlas FDA

BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS

FDA 510(k) clearance K140856 · decided 2014-05-02

Clearance details

K-number
K140856
Device name
BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS
Applicant
C.R. Bard, Inc.
Decision
Substantially Equivalent
Date received
2014-04-03
Decision date
2014-05-02
Days to decision
29 days
Clearance type
Special
Product code
KXK
Device class
2
Regulation number
892.5730
Medical specialty
Radiology
Advisory committee
Radiology
Location
Covington, GA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

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Avitene Microfibrillar Collagen Hemostat (P800002/S033)C.R. Bard, Inc.2025-03-13
AVITENE MICROFIBRILLAR COLLAGEN HEMOSTAT NON-WOVEN WEB (P800002/S032)C.R. Bard, Inc.2025-02-18
Avitene™ Bulk Flour Cleanroom Expansion (P800002/S031)C.R. Bard, Inc.2024-01-18
Avitene™ Microfibrillar Collagen Hemostat (P800002/S030)C.R. Bard, Inc.2023-10-04
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Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web and Avitene Microfibrillar Collagen Hemostat (MCH) EndoAvit (P800002/S027)C.R. Bard, Inc.2022-04-01