DEVICE: PHASOR (B775635K0)

Device Identifier (DI) Information

PHASOR
6.35K
In Commercial Distribution
6.35K
PHASOR HEALTH LLC
B775635K0
HIBCC
February 20, 2123
1
111926675 *Terms of Use
Phasor Drill 6.35-mm diameter, ~70-mm usable length with drill stop extension (tapered) + Kit (version A1) with Stapler
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Device Characteristics

MR Unsafe
No
No
Yes
Yes
No
Yes
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
44064 Neurosurgical procedure kit, medicated
A collection of various sterile neurosurgical instruments, dressings, pharmaceuticals, and the necessary materials used to perform a neurosurgical procedure. This is a single-use device.
Active false
46277 Automatic cranial perforator, single-use
A sterile, metallic rotary endpiece designed to cut a circular section, or sections, of the skull vault (calvarium) to provide access to the interior for diagnostic/therapeutic purposes or for the removal of a bone flap for brain surgery. It typically consists of two coaxial drill shafts (one rotating inside the other), a drive shank that enables connection to a powered (either electrical or pneumatic) handpiece, and a built-in clutch mechanism. The inner drill shaft extends slightly beyond the outer cutter in such a way that when the inner drill shafts penetrates the inner table of the skull the clutch mechanism disengages. This is a single-use device.
Active false
35884 Skin stapler/staple, non-bioabsorbable
A hand-held manual, surgical instrument preloaded with non-bioabsorbable skin staples designed to apply the staples to approximate the free skin edges of an incision or wound. The staples (which may be clip-like) are made of metal [e.g., stainless steel or titanium (Ti)] and intended to be removed once the wound has sufficiently healed. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K161704 000
No CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

202bbd5b-0f94-4b99-86b4-9388ab03ada3
February 28, 2023
1
February 20, 2023
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
Yes
No CLOSE

Customer Contact

[?]
8329821234
r@phasorhealth.com
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