BIOSET XC— 510(k) K060180
Substantially EquivalentRegeneration Technologies, Inc.
FDA 510(k) clearance K060180 for BIOSET XC, Substantially Equivalent on 2006-09-06. Applicant: Regeneration Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Regeneration Technologies, Inc.
- Product code
- Code MBP
- Device class
- Class 2
- Regulation
- 21 CFR 888.3045
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Alachua, FL, US
Recent devices under product code MBP
view allMore clearances from Regeneration Technologies, Inc.
view all- K080418 — REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST
- K072238 — BIOSET XCH
- K072327 — CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON
- K063584 — STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937
- K060253 — STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.
Data sourced from openFDA. This site is unofficial and independent of the FDA.